関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | L-Isoleucine | HCID 6306 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1-tert-butoxycarbonyloxy-6-chloro-1H-benzotriazole | HCID 13292852 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | tert-Butanol | HCID 6386 | — |
| 生成物 | tert-Butoxycarbonyl-L-isoleucine | HCID 2724762 | 104.7% |
反応手順
A suspension of 1-tert-butoxycarbonyloxy-6-chloro-1H-benzotriazole (2.7 g.), L-isoleucine (1.3 g) and triethylamine (3.5 ml.) in a mixture of water (8 ml.) and tert-butyl alcohol (12 ml.) was stirred for 2 hours at 60° to 62° C. tert-Butyl alcohol was distilled off from the reaction mixture under reduced pressure and water (15 ml.) was added to the residue. The mixture was adjusted to pH 3 with a citric acid aqueous solution under ice-cooling and extracted with ethyl acetate. The extract was then washed with water and a saturated sodium chloride aqueous solution. The thus formed precipitates were filtered off and then the filtrate was dried over magnesium sulfate. The solution was concentrated and a mixture of ether and petroleum ether (1:1) was added to the residue. An insoluble material was filtered off and the filtrate was concentrated under reduced pressure to give N-tert-butoxycarbonyl-L-isoleucine (2.4 g.), oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | USRE030752 |
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| 出典データセット | uspto-grants-1981_09 |
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| ORD ID | ord-deaf4431e51c4220b93d7200c2e73c0d |
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| 出典メモ | uspto-grants-1981_09 |
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