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HRID 20354作成日:2026年10月27日

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

https://huagongshe.com/reaction/20354

反応式

関与物質

役割名称HCID仕込み量
反応物Oxiranemethanol, 4-methylbenzenesulfonate, (S)-HCID 153296—
反応物HCID 178418816HCID 178418816—
溶媒TetrahydrofuranHCID 8028—
生成物Toluene-4-sulfonic acid 2-(S)-hydroxy-5-methylhexyl esterHCID 8749826975.5%

反応条件

温度2.5 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745438B2
出典データセットuspto-grants-2010_06
ORD IDord-3e73c66220eb47a0913b0234fe1c8597
出典メモuspto-grants-2010_06