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Benzyl (3-Oxopropyl)carbamate → ethyl P-(3-benzyloxycarbonylamino-1-hydroxy-propyl)-P-methyl-phosphinate

HRID 2210775
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인쇄 미리보기

반응식

HRID 2210775 반응식
[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH2:13][CH:14]=[O:15])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:16][PH:17](=[O:21])[O:18][CH2:19][CH3:20]>C(N(CC)CC)C>[CH2:1]([O:8][C:9]([NH:11][CH2:12][CH2:13][CH:14]([P:17]([CH3:16])(=[O:21])[O:18][CH2:19][CH3:20])[OH:15])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10398106Benzyl (3-Oxopropyl)carbamateHCID 178476777HCID 178476777, 화합물

생성물 1

HCID 10403409ethyl P-(3-benzyloxycarbonylamino-1-hydroxy-propyl)-P-methyl-phosphinate

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

A mixture of 5.18 g of 3-(benzyloxycarbonylamino)propionaldehyde, 2.7 g of ethyl P-methylphosphinate and 2,53 g of triethylamine is heated to 100° under an inert gas atmosphere for 2 hours. After cooling to room temperature the volatile materials are removed under reduced pressure to afford a viscous oil. Chromatography thereof on silica gel gives ethyl P-(3-benzyloxycarbonylamino-1-hydroxy-propyl)-P-methyl-phosphinate as a colourless, viscous oil.

후처리

  1. temperatureis heated to 100° under an inert gas atmosphere for 2 hours
  2. customare removed under reduced pressure
  3. customto afford a viscous oil

출처 및 근거

ORD 기록
ord-12312f5e552640b3adf4f1832cd98690
출처 데이터셋
uspto-grants-1995_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05461040

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