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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 85301생성일: 2026년 10월 25일

Chloroform → 2-[2-(2,4,6-Trimethoxyphenyl)vinyl]thiophene

https://huagongshe.com/reaction/85301

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물2,4,6-TrimethoxybenzaldehydeHCID 70019—
반응물Triphenyl(2-thienylmethyl)phosphonium BromideHCID 10741697—
반응물HCID 178506676HCID 178506676—
용매TetrahydrofuranHCID 8028—
생성물2-[2-(2,4,6-Trimethoxyphenyl)vinyl]thiopheneHCID 6800864992.8%

반응 단계

In a stream of argon, to 30 ml of tetrahydrofuran was added 0.95 g of phenyllithium (19% solution in dibutylether) (2.15 mmol). To this mixture, 0.78 g (1.98 mmol) of thiophene-2-ylmethyltriphenylphosphonium bromide was added under cooling. After the mixture was well-stirred, 0.38 g (1.98 mmol) of 2,4,6-trimethoxybenzaldehyde dissolved in 3 ml of tetrahydrofuran was added dropwise. The mixture was reacted with stirring for 1.5 hours. After the reaction mixture was poured into 70 ml of ice water, extraction with 200 ml of chloroform, washing with a saturated saline solution, drying over anhydrous magnesium sulfate, and concentration were performed. The residue was purified by silica gel chromatography to give 508 mg (yield: 92%) of 2-[2-(2,4,6-trimethoxyphenyl)vinyl]thiophene as a colorless crystal.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846955B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-aaf7754e66d54ee3b720359ff69a7970
출처 메모uspto-grants-2014_09