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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 178474954, 화합물 → HCID 178474953, 화합물

HRID 1657569
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HRID 1657569 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C@H:10]2[CH2:15][CH2:14][C@H:13]([NH:16][C:17](=[O:19])[CH3:18])[CH2:12][CH2:11]2)=[CH:6][CH:5]=1)([O-])=O>[Pt]=O.C(O)C>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([C@H:10]2[CH2:11][CH2:12][C@H:13]([NH:16][C:17](=[O:19])[CH3:18])[CH2:14][CH2:15]2)=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 178474954HCID 178474954, 화합물

생성물 1

HCID 178474953HCID 178474953, 화합물수율 87%

시약·촉매·용매 2

HCID 82844Platinum oxide (PtO)촉매HCID 702Ethanol용매

실험 절차

A mixture of 2.62 g. of trans N-[4-(p-nitrophenyl)cyclohexyl]acetamide (obtained as in Example 81) and 10 g. of Adams' platinum oxide catalyst in 150 ml. of ethanol is shaken under hydrogen (for about 10 minutes) until the theoretically required amount of the gas is absorbed. The catalyst is removed on a filter and the filtrate evaporated to dryness. The residual solid is recrystallized from aqueous methanol to give 2.03 g. (87% yield) of trans N-[4-(p-aminophenyl)cyclohexyl]acetamide having a melting point of 195° to 196.5° C.

후처리

  1. additionA mixture of 2.62 g
  2. customis absorbed
  3. customThe catalyst is removed on
  4. filtrationa filter
  5. customthe filtrate evaporated to dryness
  6. customThe residual solid is recrystallized from aqueous methanol
  7. customto give 2.03 g

출처 및 근거

ORD 기록
ord-f152d432f3ab49fe9ea7e8cb6819f930
출처 데이터셋
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03960961

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