Home Crystal structure of diethyl 2-(2-chlorophenyl)-1,3-dioxane-5,5-dicarboxylate, C16H19Cl1O6
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Crystal structure of diethyl 2-(2-chlorophenyl)-1,3-dioxane-5,5-dicarboxylate, C16H19Cl1O6

  • Lin Yuan , Min Zhang , Xian-You Yuan and Fang Liu EMAIL logo
Published/Copyright: March 16, 2018

Abstract

C16H19Cl1O6, triclinic, P1̅ (no. 2), a = 7.827(8) Å, b = 9.253(9) Å, c = 12.978(13) Å, α = 101.910(11)°, β = 100.040(11)°, γ = 110.345(10)°, V = 830.7(14) Å3, Z = 2, Rgt(F) = 0.0873, wRref(F2) = 0.0909, T = 296(2) K.

CCDC no.: 1825880

The asymmetric unit of the title crystal structure is shown in the figure. Tables 1 and 2 contain details on crystal structure and measurement conditions and a list of the atoms including atomic coordinates and displacement parameters.

Table 1:

Data collection and handling.

Crystal:Colorless block
Size:0.45 × 0.40 × 0.36 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.26 mm−1
Diffractometer, scan mode:Bruker SMART, φ and ω-scans
θmax, completeness:25°, >99%
N(hkl)measured, N(hkl)unique, Rint:7724, 2914, 0.016
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 2612
N(param)refined:210
Programs:Bruker programs [1], SHELX [2, 3], OLEX2 [4]
Table 2:

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

AtomxyzUiso*/Ueq
Cl10.49710(8)0.31396(7)0.51100(4)0.08036(19)
O20.61496(13)0.32404(10)0.76595(7)0.0376(2)
O10.57604(14)0.06040(11)0.75375(8)0.0435(2)
O60.36133(13)0.21607(12)1.05394(8)0.0434(2)
O40.73344(13)0.41942(11)1.03399(8)0.0437(2)
O30.73910(15)0.17444(13)1.00941(9)0.0522(3)
C90.48353(19)0.32145(16)0.82934(11)0.0382(3)
H9A0.35840.28860.78150.046*
H9B0.51940.42850.87750.046*
C70.5636(2)0.16858(15)0.69424(10)0.0380(3)
H70.43420.13000.64820.046*
C110.66560(18)0.26133(16)0.98590(10)0.0356(3)
C10.6979(2)0.18326(16)0.62409(11)0.0411(3)
C80.4453(2)0.04047(16)0.81845(11)0.0434(3)
H8A0.4582−0.03290.86000.052*
H8B0.3174−0.00630.77120.052*
C120.31255(19)0.17965(17)0.94631(11)0.0417(3)
C60.6794(2)0.25043(19)0.53899(12)0.0522(4)
O50.15421(15)0.13210(18)0.89003(10)0.0713(4)
C20.8475(2)0.13631(19)0.64430(13)0.0530(4)
H20.86250.09000.70060.064*
C130.9059(2)0.48609(19)1.12364(13)0.0540(4)
H13A0.96070.60241.13970.065*
H13B0.99700.44591.10140.065*
C50.8056(3)0.2708(2)0.47540(15)0.0735(6)
H50.79070.31560.41830.088*
C150.2060(2)0.1813(2)1.10553(14)0.0623(5)
H15A0.14120.06591.09140.075*
H15B0.11560.22211.07590.075*
C160.2854(3)0.2600(2)1.22466(14)0.0632(5)
H16A0.34370.37451.23810.095*
H16B0.37820.22201.25280.095*
H16C0.18580.23441.26040.095*
C30.9744(3)0.1579(2)0.58139(17)0.0726(6)
H31.07510.12710.59610.087*
C140.8679(3)0.4424(2)1.22419(13)0.0655(5)
H14A0.82540.32791.21060.098*
H14B0.77190.47601.24380.098*
H14C0.98180.49511.28300.098*
C40.9529(3)0.2242(3)0.49760(18)0.0819(6)
H41.03870.23770.45540.098*
C100.48016(18)0.20315(15)0.89746(10)0.0357(3)

Source of material

Diethyl 2,2-bis(hydroxymethyl)malonate (2.64 g, 12 mmol), 2-chlorobenzaldehyde (1.41 g, 10 mmol) and nanosolid superacid (0.1 g) were added into a mixture of N,N-dimethylformamide (12 mL) and cyclohexane (8 mL) and refluxed for 5 h at 378 K with stirring. After workup, the reaction mixture was filtrated and the organic layer was washed with water (10.3 mL) and then dried over Na2SO4. Then the white powder (2.60 g, yield 76%) was isolated after filtration and evaporation. The product was recrystallized from ethyl acetate to afford colorless crystals.

Experimental details

All hydrogen atoms were identified in difference Fourier syntheses. The Uiso values of the hydrogen atoms of methyl groups were set to 1.5Ueq(C) and the Uiso values of all other hydrogen atons were set to 1.2Ueq(C).

Discussion

Since its discovery, the aldol reaction has become one of the most actively studied and synthetically implemented reactions [5], [6], [7], which is due to the bond forming efficiency as well as rich structural properties of the reaction. We previously synthesized a series of acetal compounds [8, 9] .

Herein, a new acetal compound is reported, which was synthesized and characterized by single-crystal X-ray diffraction [2], [3], [4]. The new formed ring C7-O1-C8-C10-C9-O2 (cf. the figure) exhibits a chair conformation. In the new formed 1,3-dioxane ring, the bond lengths of O1-C7 and O2-C7 are 1.403(2) Å and 1.418(2) Å, respectively. These bond lengths as well all other geometric parameters of the title molecule are in the expected ranges.

Acknowledgements

This work was financially supported by the Scientific Research Fund of Hunan Provincial Education Department (No. 16B104), the Opening Project of Key Laboratory of Comprehensive Utilization of Advantage Plants Resources in Hunan South (No. XNZW16C01) and the Scientific Research Fund of Hunan University of Science and Engineering (No. 16XKY063), Natural Science Foundation of Hunan Province of China (2018JJ3193).

References

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Received: 2017-12-2
Accepted: 2018-3-7
Published Online: 2018-3-16
Published in Print: 2018-5-24

©2018 Lin Yuan et al., published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

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