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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 979588생성일: 2026년 10월 26일

Hexamethylenetetramine → Benzo(b)thiophene-5-carboxaldehyde

https://huagongshe.com/reaction/979588

반응식

참여 물질

역할이름HCID투입량
반응물HexamethylenetetramineHCID 4101—
반응물N-bromobutanimideHCID 67184—
반응물5-Methylbenzo(b)thiopheneHCID 84346—
촉매Benzoyl PeroxideHCID 7187—
용매Carbon TetrachlorideHCID 5943—
용매ChloroformHCID 6212—
생성물Benzo(b)thiophene-5-carboxaldehydeHCID 139097297.4%

반응 단계

Under N2, NBS (6 g, 0.034 mol) was added to a solution of 5-methylbenzo[b]thiophene (30.8 g, 0.21 mol), benzoylperoxide (1.6 g) in CCl4 (300 ml) and was heated at reflux. After 15 minutes, the remainder of the NBS (35 g, 0.2 mol) was added over a period of 5 minutes and heated at reflux for 1.5 hours. The reaction mixture was then cooled, filtered and the filtrate washed with H2O (2x), dried, filtered and concentrated to dryness. The residue was dissolved in CHCl3 (130 ml) and added to a solution of hexamethylenetetramine (33.6 g, 0.24 mol) in CHCl3 (60 ml). After 0.5 hour, the reaction mixture was cooled, filtered and the solid washed with hexane. After drying, the solid was dissolved in acetic acid-H2O (275 ml) and heated at reflux for 2 hours. Then concentrated HCl (55 ml) was added and the mixture refluxed an additional 5 minutes. After cooling, the solution was extracted with ether (3×), and the organic extracts were backwashed with saturated Na2CO3 (2×), dried, filtered, and concentrated to dryness to yield 16.4 g (48%) of product

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04668697
출처 데이터셋uspto-grants-1987_05
ORD IDord-dbb990442d21427194cccc45d6fce2bb
출처 메모uspto-grants-1987_05