Pyrrolidone carboxylic acid → 5-(((Methylsulfonyl)oxy)methyl)-2-pyrrolidinone

HRID 1635554

反応式

HRID 1635554 の反応式
[OH:1][CH2:2][CH:3]1[NH:7][C:6](=[O:8])[CH2:5][CH2:4]1.N1C(C(O)=O)CCC1=O.C(N(CC)CC)C.[CH3:25][S:26](Cl)(=[O:28])=[O:27]>ClCCl>[CH3:25][S:26]([O:1][CH2:2][CH:3]1[NH:7][C:6](=[O:8])[CH2:5][CH2:4]1)(=[O:28])=[O:27]

参加物

6

実験手順

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.

後処理

  1. filtrationThe reaction mixture was filtered
  2. customto remove triethylamine hydrochloride
  3. customthe filtrate was evaporated under reduced pressure
  4. customThe crude, oily material was purified by chromatography (silica gel; 10% methanol in chloroform)

出典と根拠

ORDレコード
ord-d29ee879b4af4e7a85f1718d928580ec
出典データセット
uspto-grants-2003_01
特許番号
US06509359B1

関連ノート

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