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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 713016생성일: 2026년 10월 25일

Hydrochloric Acid → 4-(Isopropylthio)-3-methylbenzoic acid

https://huagongshe.com/reaction/713016

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Bromo-3-methylbenzoic acidHCID 82131—
반응물Isopropyl propyl disulfideHCID 118529—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Sodium HydroxideHCID 14798—
생성물4-(Isopropylthio)-3-methylbenzoic acidHCID 5855092635.8%

반응 조건

온도-78 °C

반응 단계

Butyllithium (16 mL of 1.6 M, 25.6 mmol) was added dropwise to a mixture of 4-bromo-3-methyl-benzoic acid (2.5 g, 11.6 mmol) and THF (63 mL) at −78° C. The reaction mixture was allowed to stir at −78° C. for 30 minutes before a solution of 2-isopropyldisulfanylpropane (1.7 g, 11.6 mmol) in THF (2 mL) was added dropwise. The mixture was allowed to stir at −78° C. for 30 minutes, then 30 minutes at room temperature. The reaction mixture was then diluted with 1M aqueous sodium hydroxide (100 mL). The organic layer was discarded and the aqueous layer was acidified with 4M aqueous hydrochloric acid. The aqueous layer was then extracted 3 times with ethyl acetate. The combined extracts were dried over sodium sulfate and concentrated in vacuo. The crude material was purified by silica gel column chromatography using a gradient of 0-5% MeOH in dichloromethane to give 4-(isopropylthio)-3-methylbenzoic acid (873 mg, 18%). MS m/z calc. 210.3. found 211.2 (M+1)+. Retention time: 2.32 minutes (3 min run).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181273B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-a7a805e7a4094e098c2974dcd1c8e368
출처 메모uspto-grants-2015_11