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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20354생성일: 2026년 10월 25일

Oxiranemethanol, 4-methylbenzenesulfonate, (S)- → Toluene-4-sulfonic acid 2-(S)-hydroxy-5-methylhexyl ester

https://huagongshe.com/reaction/20354

반응식

참여 물질

역할이름HCID투입량
반응물Oxiranemethanol, 4-methylbenzenesulfonate, (S)-HCID 153296—
반응물HCID 178418816HCID 178418816—
용매TetrahydrofuranHCID 8028—
생성물Toluene-4-sulfonic acid 2-(S)-hydroxy-5-methylhexyl esterHCID 8749826975.5%

반응 조건

온도2.5 °C

반응 단계

Add dropwise over 5 minutes isobutylmagnesium bromide (4.4 mL, 8.8 mmol, 2 M in diethyl ether) to a solution of lithium tetrachlorocuprate (4.4 mL, 0.44 mmol, 0.1 M in tetrahydrofuran) cooled to −35-40° C. Dissolve (2S)-(+)-glycidyl tosylate (1.674 g, 7.73 mmol) in tetrahydrofuran (8 mL), cool to −40° C. and cannulate into the stirring Grignard reaction flask. Quench with saturated aqueous ammonium chloride (25 mL), pour supernate into saturated aqueous ammonium chloride (25 mL) and water and shake well. Wash with saturated aqueous sodium chloride, dry (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 10:90 to 25:75 ethyl acetate:hexanes) to give the desired compound (1.6711 g, 75%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745438B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3e73c66220eb47a0913b0234fe1c8597
출처 메모uspto-grants-2010_06