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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53138생성일: 2026년 10월 24일

Hydrochloric Acid → 4,4-Di(4-tolyl)-but-3-enoic acid

https://huagongshe.com/ko/reaction/53138

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Diethyl SuccinateHCID 31249—
반응물4,4'-DimethylbenzophenoneHCID 69148—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
용매tert-ButanolHCID 6386—
생성물4,4-Di(4-tolyl)-but-3-enoic acidHCID 10106981—

반응 단계

To a 500 mL round-bottomed flask equipped with condenser and nitrogen inlet were added 29.7 grams (141 mmol) 4,4'-dimethylbenzophenone and 141 mL t-butanol forming a solution, followed by 17.4 grams (155 mmol) potassium t-butoxide and 29.5 grams (170 mmol) diethyl succinate. The reaction was refluxed for 18 hours, cooled, and acidified with 6N hydrochloric acid, then poured into water and extracted with ethyl acetate. The organic layer was dried over sodium sulfate and evaporated, and the residue taken up in 200 mL glacial acetic acid. It was then treated with 70 mL 48% hydrobromic acid and refluxed for 36 hours. The reaction was cooled, partitioned between water and ethyl acetate, and the combined organic layers washed with water and brine, dried over sodium sulfate, and evaporated. The residue was chromatographed on silica gel using methylene chloride/methanol as eluant to afford the product as low melting solid, 25.0 grams (66%), Rf =0.25 in 5% methanol/methylene chloride on silica gel. This material was used directly in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05618811
출처 데이터셋uspto-grants-1997_04
ORD IDord-2eea09bb3dec46f7858b5a4bdb0b69e7
출처 메모uspto-grants-1997_04