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Benzyl Bromide → D-leucic acid benzyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzyl Bromide | HCID 7498 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | (R)-2-hydroxy-4-methylpentanoic acid | HCID 439960 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | D-leucic acid benzyl ester | HCID 9991100 | — |
反応手順
To 150 ml of tetrahydrofurane of 14.50 of D-leucic acid, 15.2 g of triethylamine and then 14.4 ml of benzyl bromide are added, and the solution was stirred for 3 hours while refluxing. The insoluble matter produced from the reaction solution was filtered off, and the filtrate was concentrated in vacuo. The obtained residue was dissolved and extracted in 150 ml of ethyl acetate. The ethyl acetate layer was washed twice with saturated bicarbonate water, twice with 1N hydrochloric acid, and twice with saturated brine sequentially, and dried over sodium sulfate anhydride, and concentrated in vacuo. The obtained oily residue was dried, and the captioned compound was obtained. Yield: 18.34 g.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05594006 |
| 出典データセット | uspto-grants-1997_01 |
| ORD ID | ord-ec3d3fd529934f85b7a05b26f0e52b1d |
| 出典メモ | uspto-grants-1997_01 |