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Pyrrolidone carboxylic acid → 5-(((Methylsulfonyl)oxy)methyl)-2-pyrrolidinone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyrrolidone carboxylic acid | HCID 499 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | 5-(Hydroxymethyl)pyrrolidin-2-one | HCID 558359 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 5-(((Methylsulfonyl)oxy)methyl)-2-pyrrolidinone | HCID 13306707 | 83.6% |
反応手順
An ice cold solution of 5-(hydroxymethyl)pyrrolidin-2-one (1.5 g, 13 mmol) prepared from 2-pyrrolidone-5-carboxylic acid (Valesinas et al., J. Org. Chem. 1992, 57, 2156-2160) in 20 mL of dichloromethane was treated with triethylamine (2.4 g, 23.5 mmol) and methylsulfonyl chloride (2.2 g, 19 mmol). The resulting solution was stirred at room temperature for 18 h. The reaction mixture was filtered to remove triethylamine hydrochloride and the filtrate was evaporated under reduced pressure. The crude, oily material was purified by chromatography (silica gel; 10% methanol in chloroform) to give 2.1 g of 5-(methanesulfonyloxymethyl)pyrrolidin-2-one as an oil which solidified upon addition of ether.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06509359B1 |
| 出典データセット | uspto-grants-2003_01 |
| ORD ID | ord-d29ee879b4af4e7a85f1718d928580ec |
| 出典メモ | uspto-grants-2003_01 |