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Sodium Hydroxide → 1,1-Dimethylethyl 2-[[4-[2-[(carboxymethyl)(2-furanylmethyl)amino]ethyl]phenyl]thio]-2-methyl-propanoate

HRID 1266514
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인쇄 미리보기

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HRID 1266514 반응식
C([O:3][C:4](=[O:32])[CH2:5][N:6]([CH2:26][C:27]1[O:28][CH:29]=[CH:30][CH:31]=1)[CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][C:12]([S:15][C:16]([CH3:25])([CH3:24])[C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])=[CH:11][CH:10]=1)C.[OH-].[Na+]>C(O)C>[C:4]([CH2:5][N:6]([CH2:26][C:27]1[O:28][CH:29]=[CH:30][CH:31]=1)[CH2:7][CH2:8][C:9]1[CH:10]=[CH:11][C:12]([S:15][C:16]([CH3:24])([CH3:25])[C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])=[CH:13][CH:14]=1)([OH:32])=[O:3]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 22708226HCID 22708226, 화합물

생성물 1

HCID 227082521,1-Dimethylethyl 2-[[4-[2-[(carboxymethyl)(2-furanylmethyl)amino]ethyl]phenyl]thio]-2-methyl-propanoate

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
80 °C

실험 절차

1.0 g of 1,1-dimethylethyl 2-[[4-[2-[(2-ethoxy-2-oxoethyl)(2-furanylmethyl)amino]-ethyl]phenyl]-thio]-2-methyl-propanoate is treated with 6.5 ml of 1 N NaOH in 10 ml of ethanol. The mixture is stirred at 80° C. for 1 h, concentrated, dissolved in water and acidified with 1 N HCl. Three extractions with ethyl acetate and chromatography (dichloromethane/methanol 5+1) gives 744 mg as a colourless oil.

후처리

  1. concentrationconcentrated
  2. dissolutiondissolved in water
  3. extractionThree extractions with ethyl acetate and chromatography (dichloromethane/methanol 5+1)
  4. customgives 744 mg as a colourless oil

출처 및 근거

ORD 기록
ord-51d17c4cba9745bd8a07072cb5ff8738
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06548538B2

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