Home Crystal structure of (6aR,6a1S,10aS)-2,4a,6a,6a1,9,10-hexahydro-7H-4,5-methanocyclobuta[4,5]naphtho[8a,1-b]pyran, C15H16O
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Crystal structure of (6aR,6a1S,10aS)-2,4a,6a,6a1,9,10-hexahydro-7H-4,5-methanocyclobuta[4,5]naphtho[8a,1-b]pyran, C15H16O

  • Shengxian Zhai ORCID logo , Lunjian Chen EMAIL logo , Yongsheng Niu and Chuchu Han
Published/Copyright: July 23, 2020

Abstract

C15H16O, monoclinic, P21/c (no. 14), a = 5.4371(7) Å, b = 17.567(2) Å, c = 11.8840(18) Å, β = 101.043(9)°, V = 1114.1(3) Å3, Z = 4, Rgt(F) = 0.0422, wRref(F2) = 0.1155, T = 296(2) K.

CCDC no.: 2014890

The asymmetric unit of the molecular structure is shown in the figure. Table 1 contains crystallographic data and Table 2 contains the list of the atoms including atomic coordinates and displacement parameters.

Table 1:

Data collection and handling.

Crystal:Colorless block
Size:0.21 × 0.14 × 0.12 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.08 mm−1
Diffractometer, scan mode:Bruker APEX-II, φ and ω
θmax, completeness:28.3°, >99%
N(hkl)measured, N(hkl)unique, Rint:10178, 2747, 0.021
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 2314
N(param)refined:145
Programs:Bruker [1], Olex2 [2]
Table 2:

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2).

AtomxyzUiso*/Ueq
C10.5780(2)0.37047(7)0.56543(9)0.0364(3)
H1A0.61400.32760.51970.044*
H1B0.41160.38880.53240.044*
O10.38400(14)0.28689(5)0.68690(7)0.0370(2)
C20.7677(2)0.43389(8)0.55803(10)0.0441(3)
H2A0.92920.41110.55590.053*
H2B0.71470.46160.48690.053*
C30.7975(3)0.48893(8)0.65613(12)0.0476(3)
H30.90450.53040.65800.057*
C40.6728(3)0.47884(7)0.73964(11)0.0423(3)
C50.6903(4)0.50384(8)0.86299(13)0.0610(4)
H5A0.57200.54340.87330.073*
H5B0.85870.51650.90220.073*
C60.6041(3)0.42121(8)0.88802(11)0.0457(3)
H60.46380.42160.92900.055*
C70.8048(3)0.36707(8)0.94025(10)0.0447(3)
H70.85540.36541.01950.054*
C80.9119(2)0.32140(7)0.87562(10)0.0377(3)
C90.5133(2)0.41098(7)0.75495(10)0.0348(3)
H90.33500.42350.73240.042*
C100.57851(18)0.34258(6)0.68846(9)0.0287(2)
C110.83073(19)0.31034(6)0.74726(9)0.0304(2)
H110.96440.32430.70630.037*
C121.0343(3)0.24295(8)0.88981(12)0.0458(3)
H12A1.00750.21470.95660.055*
H12B1.20820.24170.88140.055*
C130.8437(2)0.22714(7)0.77995(11)0.0386(3)
C140.6581(3)0.17947(7)0.74542(12)0.0459(3)
H140.65930.12990.77290.055*
C150.4435(2)0.21056(7)0.65847(12)0.0447(3)
H15A0.48790.21010.58320.054*
H15B0.29760.17840.65570.054*

Source of material

All reactions were carried out under argon atmosphere with dry solvents under anhydrous conditions, unless otherwise noted. All the chemicals were purchased commercially, and used without further purification. To a solution of (4aS,5S,6aS,6a1S,10aS)-4a,5,6a,6a1,9,10-hexahydro-7H-4,5-methanocyclobuta[4,5]naphtho[8a,1-b]pyran-6(2H)-one (456.0 mg, 2.0 mmol) in absolute dry MeOH (10 mL) was added NaBH4 (151.32 mg, 4,0 mmol, 2.0 equiv) at 0 °C. The reaction mixture was stirred at this temperature for another 1 h, then the reaction mixture was warmed to room temperature. After the starting material disappeared (detected by TLC), the reaction was quenched with saturated aq. NH4Cl, and the mixture was extracted with ethyl acetate three times, and the organic layer was washed with saturated aq. NaCl solution. This organic mixture was dried over anhydrous Na2SO4, then concentrated under reduced pressure. The resulting residue was purified by flash column chromatography using petroleum ether/ethyl acetate eluent to afford the alcohol (414.5 mg, 90% yield) as a colorless sticky oil.

To a stirred solution of the intermediate alcohol (230 mg, 1.0 mmol) obtained above, and PPh3 (1310.2 mg, 5.0 mmol) in THF (20.0 mL) was added DEAD (870.7 mg, 5.0 mmol) dropwise at 0 °C. The resulting mixture was stirred at room temperature overnight before it was quenched with saturated aq. NaHCO3 solution (20 mL) and extracted with ethyl acetate (3 × 10 mL). The combined organic phases were washed with brine (20 mL) and dried over anhydrous Na2SO4. After filtration and evaporation of the solvent, the residue so obtained was purified by flash column chromatography with petroleum ether/EtOAc (15:1 to 10:1) to give the desired product (180 mg, 85%) as a foam solid. The titled crystal could be afforded by slowly evaporation of the foam solid obtained above in petroleum ether/ethyl acetate mixture.

Experimental details

Hydrogen atoms were placed in their geometrically idealized positions and constrained to ride on their parent atoms.

Comment

The polycyclic compounds are widely found in natural products [3], drug molecules [4] and bioactive compounds, [5] and due to the complicated structure and potential biological activity, the development of new methods for the synthesis of novel polycyclic compounds is of great insterest. As part of our continuing efforts on the efficient synthetic methods for cyclic compounds synthesis, [6] herein, we report a useful method and the crystal structure of the titled compound.

There is one molecule in the asymmetric unit of the title structure (see the figure). The single crystal structure verifies that all bond lengths are in normal ranges. Furthermore, the crystal packing doesn’t exhibit intramolecular or intermolecular hydrogen bonds.

Acknowledgements

This work was supported by the Foundation of Henan postdoctoral foundation and the postdoctoral innovation base of Anyang Institute of Technology.

References

1. BRUKER. SAINT, APEX2 and SADABS. Bruker AXS Inc., Madison, WI, USA (2009).Search in Google Scholar

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3. Liao, H.-B.; Lei, C.; Gao, L.-X.; Li, J.-Y.; Li, J.; Hou, A.-J.: Two enantiomeric pairs of meroterpenoids from Rhododendron capitatum. Org. Lett. 17 (2015) 5040–5043.10.1021/acs.orglett.5b02515Search in Google Scholar PubMed

4. Hoffmann-Röder, A.; Krause, N.: Synthesis and properties of allenic natural products and pharmaceuticals. Angew. Chem. Int. Ed. 43 (2004) 1196–1216.10.1002/anie.200300628Search in Google Scholar PubMed

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6. Zhai, S.; Qiu, S.; Chen, L.; Niu, Y.; Yu, Y.; Yang, B.; Zhang, B.; Han, C.; Yang, L.; Zhai, H.: Synthesis of cyclobutane-fused oxygen-containing tricyclic framework via thermally promoted intramolecular cycloaddition of cyclohexadienone-tethered allenes. Chem. Commun. 56 (2020) 3405–3408.10.1039/D0CC00061BSearch in Google Scholar

Received: 2020-06-22
Accepted: 2020-07-08
Published Online: 2020-07-23
Published in Print: 2020-10-27

©2020 Shengxian Zhai et al., published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 International License.

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  78. Crystal structure of (2-carboxy-4-(3-carboxy-5-carboxylatophenoxy)benzoato-κ2O,O′)bis(1,10-phenantroline-κ2N,N′)cobalt(II), C40H24N4O9Co
  79. The crystal structure of (3S,8R,10R,14R)-17-((2S,5S)-5-(2-hydroxypropan-2-yl)-2-methyltetrahydrofuran-2-yl)-4,4,8,10,14-pentamethyl-12-oxohexadecahydro-1H-cyclopenta[a]phenanthren-3-yl acetate, C32H52O5
  80. Crystal structure of (μ2-1,1′-bis(diphenylphosphino)ferrocene-κ2P,P′)-bis[(Z)N-(3-fluorophenyl)-O-methylthiocarbamato-S]digold(I) chloroform solvate, C50H42Au2F2FeN2O2P2S2, CHCl3
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