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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1628169생성일: 2026년 10월 27일

Borane;tetrahydrofuran → 2-(4-Hydroxymethyl-phenylsulfanylmethyl)-benzoic acid 2,2,2-trichloro-ethyl ester

https://huagongshe.com/reaction/1628169

반응식

참여 물질

역할이름HCID투입량
반응물Borane;tetrahydrofuranHCID 2723981—
반응물2-(4-Carboxy-phenylsulfanylmethyl)-benzoic acid 2,2,2-trichloro-ethyl esterHCID 66865243—
용매TetrahydrofuranHCID 8028—
생성물2-(4-Hydroxymethyl-phenylsulfanylmethyl)-benzoic acid 2,2,2-trichloro-ethyl esterHCID 6686525491%

반응 조건

온도0 °C

반응 단계

To a solution of 2-(4-Carboxy-phenylsulfanylmethyl)-benzoic acid 2,2,2-trichloro-ethyl ester (80 mg, 0.191 mmol) in THF (1 mL) at 0° C. was added dropwise BH3-THF (0.4 mL, 1.0M solution in THF). The reaction was stirred at 0° C. for 0.5 h after the addition was complete, thereafter the cooling bath was removed and the reaction was stirred for 2 h at rt. The reaction was quenched at 0° C. by careful addition of THF/H2O, 80/20 followed by dropwise addition of 2M HCl. The mixture was stirred for an additional 10 minutes and thereafter diluted with water. THF was removed and the water phase was extracted with DCM and the combined organic phase was dried through a phase separator and concentrated to give the titled compound (70 mg, 91%) as an oil; 1H NMR (400 MHz, CDCl3): δ 4.53 (s, 2H), 4.64 (s, 2H), 4.94 (s, 2H), 7.19-7.30 (m, 5H), 7.30-7.36 (m, 1H), 7.37-7.44 (m, 1H), 8.06 (d, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08785681B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-79912b9f8e914994ae18e2e79eadbdd6
출처 메모uspto-grants-2014_07