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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 70167927, 화합물

HRID 2188203
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인쇄 미리보기

반응식

HRID 2188203 반응식
C([CH2:8][NH:9][CH2:10][C:11]1[CH2:20][CH2:19][C:18]2[C:13](=[CH:14][CH:15]=[C:16]([F:21])[CH:17]=2)[C:12]=1[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)C1C=CC=CC=1.[ClH:28]>C(O)C.[Pd]>[ClH:28].[F:21][C:16]1[CH:17]=[C:18]2[C:13](=[CH:14][CH:15]=1)[C@@H:12]([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[C@@H:11]([CH2:10][NH:9][CH3:8])[CH2:20][CH2:19]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 18477085HCID 18477085, 화합물

생성물 1

HCID 70167927HCID 70167927, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To a mixture of 2-(N-benzylmethylamino)methyl-6-fluoro-1-phenyl-3,4-dihydronaphthalene (0.95 g) in ethyl alcohol (50 cm3) and hydrochloric acid (5 M, 1 cm3) was added palladium on charcoal (5%, 0.25 g). The resultant mixture was stirred under an atmosphere of hydrogen at a pressure of 2 atm at room temperature for 60 h. The catalyst was removed by filtration through a pad of Dicalite® and the solvent was evaporated under reduced pressure to provide the title compound (0.75 g) as a white solid.

후처리

  1. customThe catalyst was removed by filtration through a pad of Dicalite®
  2. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-76a0d8a0d52548969fe6864a4c4b764f
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06410592B1

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