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3-Phenyl-8-carbobenzyloxy-1-oxa-3,8-diazaspiro[4.5]decan-2-one → 3-Phenyl-1-oxa-3,8-diazaspiro(4.5)decan-2-one

HRID 127263
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인쇄 미리보기

반응식

HRID 127263 반응식
[C:1]1([N:7]2[CH2:11][C:10]3([CH2:16][CH2:15][N:14](C(OCC4C=CC=CC=4)=O)[CH2:13][CH2:12]3)[O:9][C:8]2=[O:27])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>[Pd].C(O)C>[C:1]1([N:7]2[CH2:11][C:10]3([CH2:12][CH2:13][NH:14][CH2:15][CH2:16]3)[O:9][C:8]2=[O:27])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 130165993-Phenyl-8-carbobenzyloxy-1-oxa-3,8-diazaspiro[4.5]decan-2-one

생성물 1

HCID 202864753-Phenyl-1-oxa-3,8-diazaspiro(4.5)decan-2-one수율 113.7%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A mixture of 3.4 g 3-phenyl-8-carbobenzyloxy-1-oxa-3,8-diazaspiro[4.5]decan-2-one, 50 ml ethanol and 0.4 g, 10% palladium on carbon is hydrogenated at room temperature and 60 psi for 6 hours. Filtration and removal of solvent affords 2.45 g 3-phenyl-1-oxa-3,8-diazaspiro[4.5]decan-2-one, a pasty solid; m/e=232 (M+).

후처리

  1. customis hydrogenated at room temperature
  2. filtrationFiltration and removal of solvent

출처 및 근거

ORD 기록
ord-f3a5034792e44fde8096656c9dfa7030
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04255432

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