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Hexane → N-((Phenylmethoxy)carbonyl)-L-serine methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hexane | HCID 8058 | — |
| 反応物 | N-(Benzyloxycarbonyl)-L-serine | HCID 100310 | — |
| 反応物 | Trimethylsilyldiazomethane | HCID 167693 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | N-((Phenylmethoxy)carbonyl)-L-serine methyl ester | HCID 6999535 | 100% |
反応手順
To a solution of N-carbobenzyloxy-L-serine (4.0 g, 16.7 mmol) in benzene (200 ml) and methanol (50 ml) was added a solution of 2M trimethylsilyldiazomethane in hexane (10.9 ml, 21.7 mmol) in an ice bath, and the mixture was stirred at room temperature for 3 hours. After checking the completion of the reaction, the reaction mixture was concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (1:1→1:3) as the eluant to afford N-carbobenzyloxy-L-serine methyl ester (4.40 g, yield 100%) as a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07001897B2 |
| 出典データセット | uspto-grants-2006_02 |
| ORD ID | ord-4b434369fbc940f9a0701f5badd41222 |
| 出典メモ | uspto-grants-2006_02 |