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

HRID 622810
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HRID 622810 반응식
[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]
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참가 물질

6

반응물 3

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

생성물 1

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

시약·촉매·용매 2

HCID 702Ethanol용매2회HCID 962
Water
용매
2회

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-8fcb660784cc4e6b9a9b9209d3b81a96
출처 데이터셋
uspto-grants-1988_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04772692

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