The title compound, C 16 H 14 O 2 S, was prepared by the oxidation of 3,5-dimethyl-2-phenyl-1-benzofuran using 3chloroperbenzoic acid. The O atom and the methyl group of the methylsulfinyl substituent lie on opposite sides of the plane of the benzofuran fragment. The phenyl ring is rotated out of th
2-Methyl-3-methylsulfinyl-5-phenyl-1-benzofuran
✍ Scribed by Choi, Hong Dae ;Seo, Pil Ja ;Lee, Hee Kyung ;Son, Byeng Wha ;Lee, Uk
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 97 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
The title compound, C 16 H 14 O 2 S, was prepared by oxidation of 2-methyl-3-methylsulfanyl-5-phenyl-1-benzofuran using 3chloroperbenzoic acid. Shortstacking distances are prevented by the steric influence of the methylsulfinyl group.
📜 SIMILAR VOLUMES
The title compound, C~15~H~11~ClO~2~S, was prepared by the oxidation of 5-chloro-3-methylsulfanyl-2-phenyl-1-benzofuran using 3-chloroperbenzoic acid. The 1-benzofuran ring system is almost planar. The crystal structure is stabilized by weak aromatic π–π stacking and –CH~2~—H...π interactions.
The title compound, C~15~H~11~BrO~2~S, was prepared by oxidation of 5-bromo-3-methylsulfanyl-2-phenyl-1-benzofuran using 3-chloroperbenzoic acid. The crystal structure is stabilized by aromatic π–π stacking and CH~2~—H...π interactions.
The title compound, C 10 H 9 ClO 2 S, was prepared by the oxidation of 5-chloro-2-methyl-3-methylsulfanyl-1-benzofuran using 3-chloroperbenzoic acid. The benzofuran ring system is almost planar. Noor -CH 2 -HÁ Á Á interactions were observed.
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.