The title compound, C~13~H~15~BrO~3~, was synthesized by the reaction of ethyl 3-(2,3-dihydro-1-benzofuran-5-yl)propanoate with bromine. The benzofuran system is planar and subtends an angle of 87.27 (9)° with the propanoate unit.
2,3-Dihydro-2,2-dimethylbenzofuran-7-yl N-methylcarbamate
✍ Scribed by Xu, Liang-Zhong ;Yu, Guan-Ping ;Yang, Shuang-Hua
- Publisher
- International Union of Crystallography
- Year
- 2005
- Tongue
- English
- Weight
- 152 KB
- Volume
- 61
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C 12 H 15 NO 3 , crystallizes with two independent molecules in the asymmetric unit. The bond lengths and angles in both molecules are within normal ranges. There are some weak intermolecular hydrogen-bond interactions in the crystal structure, which provide stabilization.
📜 SIMILAR VOLUMES
In the title compound, C 24 H 38 N 2 O 6 S 2 , which was synthesized from (+)-10-camphorsulfonic acid chloride and piperazine, the central piperazine ring adopts a chair conformation. The two camphorlsulfonyl groups are bound to the piperazine N atoms in equatorial positions. The molecule has approx
The title compound, C 11 H 12 O 2 S, was prepared by the oxidation of 2,5-dimethyl-3-methylsulfanyl-1-benzofuran using 3-chloroperbenzoic acid. The 1-benzofuran ring system is essentially planar. The crystal structure is stabilized by-CH 2 -HÁ Á Á interactions.