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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
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 178418816 | HCID 178418816 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Toluene-4-sulfonic acid 2-(S)-hydroxy-5-methylhexyl ester | HCID 87498269 | 75.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07745438B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-3e73c66220eb47a0913b0234fe1c8597 |
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| 出典メモ | uspto-grants-2010_06 |
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