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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 359149생성일: 2026년 10월 24일

Dibenzyl sulfide → HCID 15078741, 화합물

https://huagongshe.com/ko/reaction/359149

반응식

참여 물질

역할이름HCID투입량
반응물Dibenzyl sulfideHCID 10867—
반응물Sodium hydrideHCID 24758—
반응물alpha,beta-Diphenyl acrylic acidHCID 66677—
반응물Methyl phenylglyoxalateHCID 84835—
반응물Thiomandelic acidHCID 10464709—
용매DimethylformamideHCID 6228—
생성물HCID 15078741HCID 15078741—

반응 조건

온도60 °C

반응 단계

To an ice cooled, stirred solution of dibenzyl sulfide (2.14 g, 0.01 m) in dried N,N-dimethylformamide was added sodium hydride (0.88 g, 0.022 mmol of a 60% suspension in mineral oil). The mixture was gradually heated to 60° C. (bath temperature), kept 2 hours and allowed to cool. Methyl benzoylformate (1.42 ml, 0.01 mmol) was then added and the mixture heated at 60° C. for 1 hour, cooled, added to a stirred ice-dilute hydrochloric acid-ether mixture, separated, the aqueous layer re-extracted 1 time with ether, and the combined organic layer washed 2 times with water, dried over sodium sulfate, filtered and concentrated to a residue. Chromatography on silica gel (1 time flush with 10% ethyl acetate/hexane followed by a careful chromatography with a methylene chloride/hexane mixture) yielded 50 mg. of product compound as a pale yellow-white crystalline material. M.S.: M+ =328; NMR: consistent, identical to the nmr spectrum of material prepared from α-phenylcinnamic acid and α-mercaptophenylacetic acid via Michael addition and ring closure. ##STR28##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04999436
출처 데이터셋uspto-grants-1991_03
ORD IDord-97aaa44cbbea4bb3b94f1c2bc649136e
출처 메모uspto-grants-1991_03