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Dicyclohexylcarbodiimide → HCID 20344450, 화합물

HRID 1704785
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HRID 1704785 반응식
C1(N=C=NC2CCCCC2)CCCCC1.[C:16]([S:19][CH2:20][CH:21]([CH2:25][C:26](=O)[NH2:27])[C:22]([OH:24])=[O:23])(=[O:18])[CH3:17]>N1C=CC=CC=1>[C:16]([S:19][CH2:20][CH:21]([CH2:25][C:26]#[N:27])[C:22]([OH:24])=[O:23])(=[O:18])[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10868DicyclohexylcarbodiimideHCID 203444533-Acetylthio-2-carbamoylmethylpropanoic acid

생성물 1

HCID 20344450HCID 20344450, 화합물

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

Dicyclohexylcarbodiimide (1.03 g.) is added to a solution of 3-acetylthio-2-carbamoylmethylpropanoic acid (1.02 g.) in pyridine (18 ml.). After five hours stirring at room temperature, the precipitate is filtered off and the filtrate is concentrated in dryness, the residue is dissolved in ethyl acetate and extracted with saturated aqueous bicarbonate. The aqueous phase is acidified and extracted with ethyl acetate. This organic layer is dried and concentrated to dryness. The residue, 3-acetylthio-2-cyanomethylpropanoic acid is crystallized from ether-hexane, m.p. 110°-112°.

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후처리

  1. filtrationthe precipitate is filtered off
  2. concentrationthe filtrate is concentrated in dryness
  3. dissolutionthe residue is dissolved in ethyl acetate
  4. extractionextracted with saturated aqueous bicarbonate
  5. extractionextracted with ethyl acetate
  6. customThis organic layer is dried
  7. concentrationconcentrated to dryness
  8. customThe residue, 3-acetylthio-2-cyanomethylpropanoic acid is crystallized from ether-hexane, m.p. 110°-112°

출처 및 근거

ORD 기록
ord-67d49b8e20ef4db3b054928e8b979c87
출처 데이터셋
uspto-grants-1978_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04127729

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