関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Lithium borohydride | HCID 4148881 | — |
| 反応物 | (3R,5S)-5-(hydroxymethyl)-1-tosylpyrrolidin-3-ol | HCID 11265723 | — |
| 反応物 | N-tosylhydroxy-L-proline methyl ester | HCID 18640953 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | N-Tosylhydroxy-L-prolinol | HCID 67796897 | 88.8% |
反応手順
(2S,4R)-1-(4-toluenesulfonyl)-2-hydroxymethyl-4-hydroxy pyrrolidine. To a solution of N-tosylhydroxy-L-proline methyl ester (62.20 g, 0.21 mole) in THF (600 mL) at 0° C. was added LiBH4 (15.8 g, 0.73 mole) in small portions. The reaction mixture was stirred at 0° C. for 1 h and allowed to stand at 23° C. for 18 h. The reaction mixture was cooled to -20° C., made neutral with 6N HCl and concentrated under reduced pressure. The residue was treated with water (550 ml) and extracted with EtOAc (4×300 mL). The combined organic extracts were washed with H2O, dried over MgSO4, filtered and concentrated under reduced pressure to give N-tosylhydroxy-L-prolinol as a white solid (50.56 g, 88.8%) which was used in the next step without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04994460 |
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| 出典データセット | uspto-grants-1991_02 |
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| ORD ID | ord-a7d70a7f216e4b2a979841fd9943d525 |
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| 出典メモ | uspto-grants-1991_02 |
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