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1,1-Dimethylethyl 4-(hydroxyimino)-4-phenylbutylcarbamate → tert-butyl N-(4-amino-4-phenylbutyl)carbamate

HRID 352112
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인쇄 미리보기

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HRID 352112 반응식
O[N:2]=[C:3]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH2:4][CH2:5][CH2:6][NH:7][C:8](=[O:14])[O:9][C:10]([CH3:13])([CH3:12])[CH3:11]>C(O)C.[Pd]>[NH2:2][CH:3]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH2:4][CH2:5][CH2:6][NH:7][C:8](=[O:14])[O:9][C:10]([CH3:13])([CH3:11])[CH3:12]
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참가 물질

4

반응물 1

HCID 739931561,1-Dimethylethyl 4-(hydroxyimino)-4-phenylbutylcarbamate

생성물 1

HCID 16795070tert-butyl N-(4-amino-4-phenylbutyl)carbamate수율 107.6%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

1,1-Dimethylethyl 4-(hydroxyimino)-4-phenylbutylcarbamate (2.3 g, 8.3 mmol), in absolute ethanol was hydrogenated over 10% palladium on charcoal (0.5 g) at 5 bar pressure for 20 h. The mixture was then filtered and the filtrate concentrated to dryness to afford the title compound as a colourless oil (2.36 g).

후처리

  1. filtrationThe mixture was then filtered
  2. concentrationthe filtrate concentrated to dryness

출처 및 근거

ORD 기록
ord-67fc204a87ee4cd9ade8e6b1f0e75ae7
출처 데이터셋
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06743939B2

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