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Dichloromethane → (4-Allylthio-3-ethylazetidin-2-on-1-yl)acetic acid

HRID 622810
ノート
印刷プレビュー

反応式

HRID 622810 の反応式
[CH2:1]([S:4][CH:5]1[N:8]([CH2:9][C:10]([O:12]C)=[O:11])[C:7](=[O:14])[CH:6]1[CH2:15][CH3:16])[CH:2]=[CH2:3].[OH-].[K+].ClCCl>C(O)C.O>[CH2:1]([S:4][CH:5]1[N:8]([CH2:9][C:10]([OH:12])=[O:11])[C:7](=[O:14])[CH:6]1[CH2:15][CH3:16])[CH:2]=[CH2:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6344DichloromethaneHCID 14797Potassium HydroxideHCID 13106494Methyl (4-allylthio-3-ethylazetidin-2-on-1-yl)acetate

生成物 1

HCID 13106496(4-Allylthio-3-ethylazetidin-2-on-1-yl)acetic acid収率 90.6%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒2 回HCID 962
Water
溶媒
2 回

実験手順

To a stirred solution of 3 g of methyl 2-(4-allylthio-3-ethylazetidin-2-on-1-yl)acetate in 10 ml of absolute ethanol was added dropwise a solution of 0.9 g of potassium hydroxide in a mixture of 12 ml of ethanol and 1 ml of water. After 5 minutes, the mixture was poured into a mixture of 10 ml of dichloromethane and 20 ml of water. After acidification with 13 ml of 2M HCl, the mixture was extracted with further dichloromethane; the dichloromethane extracts were extracted with saturated sodium bicarbonate solution. These aqueous extracts were acidified to pH 1.5 with 5M HCl and then extracted with dichloromethane. These organic extracts were evaporated to dryness to afford the title compound as a white crystalline solid (2.56 g).

後処理

  1. extractionAfter acidification with 13 ml of 2M HCl, the mixture was extracted with further dichloromethane
  2. extractionthe dichloromethane extracts were extracted with saturated sodium bicarbonate solution
  3. extractionextracted with dichloromethane
  4. customThese organic extracts were evaporated to dryness

出典と根拠

ORDレコード
ord-8fcb660784cc4e6b9a9b9209d3b81a96
出典データセット
uspto-grants-1988_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04772692

反応ノート

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