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tert-Butyl [3-(benzyloxy)cyclobutyl]carbamate → tert-Butyl (3-hydroxycyclobutyl)carbamate

HRID 2112092
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인쇄 미리보기

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HRID 2112092 반응식
C([O:8][CH:9]1[CH2:12][CH:11]([NH:13][C:14](=[O:20])[O:15][C:16]([CH3:19])([CH3:18])[CH3:17])[CH2:10]1)C1C=CC=CC=1>CO.[OH-].[Pd+2].[OH-]>[OH:8][CH:9]1[CH2:10][CH:11]([NH:13][C:14](=[O:20])[O:15][C:16]([CH3:18])([CH3:17])[CH3:19])[CH2:12]1
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참가 물질

4

반응물 1

HCID 53415284tert-Butyl [3-(benzyloxy)cyclobutyl]carbamate

생성물 1

HCID 22594430tert-Butyl (3-hydroxycyclobutyl)carbamate

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 887Methanol용매

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온도
45 °C

실험 절차

2.77 g (10 mmol) tert.butyl (3-benzyloxy-cyclobutyl)-carbamate are suspended in 100 ml of methanol and combined with 200 mg palladium hydroxide. The reaction mixture is stirred for 5 h at 45° C. and 45 bar H2 pressure. Then the catalyst is filtered off and the solvent is eliminated in vacuo. The residue is taken up in chloroform and washed three times with aqueous sodium hydrogen carbonate solution. The organic phase is dried with magnesium sulphate and the solvent is eliminated in vacuo.

후처리

  1. filtrationThen the catalyst is filtered off
  2. washwashed three times with aqueous sodium hydrogen carbonate solution
  3. dry with materialThe organic phase is dried with magnesium sulphate

출처 및 근거

ORD 기록
ord-2ce3e629d74f48249c2bb4dd59c50ac9
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07521457B2

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