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Trityl chloride → N-triphenylmethyl-alpha-aminobutyrolactone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trityl chloride | HCID 6456 | — |
| 反応物 | 4-Methylmorpholine | HCID 7972 | — |
| 反応物 | Homoserine lactone hydrobromide | HCID 73508 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-triphenylmethyl-alpha-aminobutyrolactone | HCID 13856082 | — |
反応手順
α-Aminobutyrolactone hydrobromide (10.0 g, 54.9 mmol), N-methylmorpholine (11.2 g, 110.0 mmol) and triphenylmethyl chloride (15.4 g, 55.2 mmol) were dissolved in N,N-dimethylformamide (DMF) (200 ml) (distilled from calcium hydride) and stirred at ambient temperature for 16 hours. The mixture was filtered, and water (200 ml) was added to the DMF-solution. The resulting slurry was stirred for 2 hours, the precipitate was filtered off and washed with a mixutre of DMF and water (1:1, 50 ml). The solid was resuspended in water (100 ml), filtered and dried at 50° C. in vacuo. N-triphenylmethyl-α-amino-butyrolactone was isolated as a white solid. Yield 17.55 g (93.2%), mp 164.5°-165.5° C. (uncorrected).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05419893 |
| 出典データセット | uspto-grants-1995_05 |
| ORD ID | ord-53b464ac8a92404eaf0cf1fbc086b494 |
| 出典メモ | uspto-grants-1995_05 |