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Diethyl Ether → (2S)-2-t-Butoxycarbonylamino-3-n-hexanoyloxy-2-methyl-1-propanal
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | (2R)-2-t-Butoxycarbonylamino-3-n-hexanoyloxy-2-methyl-1-propanol | HCID 11630856 | — |
| 反応物 | HCID 178418287 | HCID 178418287 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (2S)-2-t-Butoxycarbonylamino-3-n-hexanoyloxy-2-methyl-1-propanal | HCID 20721242 | 95% |
反応手順
Molecular sieve 4A (220 g) and pyridinium chlorochromate (43.6 g, 0.202 mol) were added to a solution of (2R)-2-t-butoxycarbonylamino-3-n-hexanoyloxy-2-methyl-1-propanol (30.7 g, 0.101 mol) obtained in Reference example 1 (1a) in methylene chloride (600 mL) under ice-cooling and the mixture was stirred at room temperature for 2 hours. Ether was added to the reaction mixture, the mixture was filtered and the filtrate was evaporated under reduced pressure. The residue was purified by silica gel chromatography (hexane:ethyl acetate, 10:1-5:1) to obtain the title compound (28.8 g, yield: 95%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07910617B2 |
| 出典データセット | uspto-grants-2011_03 |
| ORD ID | ord-ef9800e3a3694b34a9aa7b891b4d8a93 |
| 出典メモ | uspto-grants-2011_03 |