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3-Benzyloxybenzyl bromide → 2(R)-isopropyl-3-(3-benzyloxyphenyl)-propanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Benzyloxybenzyl bromide | HCID 1502047 | — |
| 反応物 | 3-Acetoxy-4-tert-butylbenzyl bromide | HCID 21458757 | — |
| 反応物 | N-tert-butoxycabonyl-2(R)-methyl-4(S)-hydroxy-5(S)-amino-7(S)-isopropyl-8-(3-hydroxyphenyl)-octanoic acid (N-butyl)-amide | HCID 131719571 | — |
| 溶媒 | Methylenechloride Hexane | HCID 21226440 | — |
| 生成物 | 2(R)-isopropyl-3-(3-benzyloxyphenyl)-propanol | HCID 22865734 | — |
反応手順
The N-tert-butoxycarbonyl-2(R)-methyl-4(S)-hydroxy-5(S)-amino-7(S)-isopropyl-8-(3-hydroxyphenyl)-octanoic acid (N-butyl)amide used as starting material is prepared analogously to Example 5a)-5l), except that in step k) instead of 3-acetoxy-4-tert-butyl-benzyl bromide there is used 3-benzyloxy-benzyl bromide, so that in step i) 2(R)-isopropyl-3-(3-benzyloxy-phenyl)-propanol, Rf (dichloromethane/hexane=1:1)=0.19, is obtained directly.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05559111 |
| 出典データセット | uspto-grants-1996_09 |
| ORD ID | ord-d19dc6469b77442f95cb8bb3599466b6 |
| 出典メモ | uspto-grants-1996_09 |