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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37517생성일: 2026년 10월 23일

Trimethyl borate → 4-(Methylthio)phenylboronic acid

https://huagongshe.com/ko/reaction/37517

반응식

참여 물질

역할이름HCID투입량
반응물Trimethyl borateHCID 8470—
반응물Sodium HydroxideHCID 14798—
반응물4-BromothioanisoleHCID 66037—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물4-(Methylthio)phenylboronic acidHCID 273395983.3%

반응 단계

Under nitrogen, a stirred solution of 30 g (150 mmol) of 4-bromothioanisole (Aldrich) in 1500 mL of anhydrous THF at -78 ° C. was treated with 180 mmol of n-butyllithium in hexane. After 30 minutes, 51 mL (450 mmol) of trimethylborate was added neat and the reaction was allowed to warm to ambient temperature overnight. A solution of 300 mL of 10% NaOH was added and the mixture stirred vigorously for lb. The solvent was removed in vacuo, the pH adjusted to 4-5, and the product collected by filtration. Repeated washings with hexane and water provided 21 g (83%) of 4-methylthiophenylboronic acid (21 in Synthetic Scheme VII when R5 =SCH3 and R3, R4, R6, and R7 =H) as a colorless solid: NMR (DMSO-d6) d 2.47 (s, 3H), 7.20 (d, J=8 Hz, 2H), 7.71 (d, J=8 Hz, 2H), 7.96 (br s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420287
출처 데이터셋uspto-grants-1995_05
ORD IDord-2b95209fadce47fba1a904e47c6976a4
출처 메모uspto-grants-1995_05