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1-Pentyne → 2-(Benzyloxy)-6-(2-n-propylethynyl)naphthalene

HRID 493039
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인쇄 미리보기

반응식

HRID 493039 반응식
[CH2:1]([O:8][C:9]1[CH:18]=[CH:17][C:16]2[C:11](=[CH:12][CH:13]=[C:14](Br)[CH:15]=2)[CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:20]#[C:21][CH2:22][CH2:23][CH3:24].C[Si](C#C)(C)C>>[CH2:1]([O:8][C:9]1[CH:18]=[CH:17][C:16]2[C:11](=[CH:12][CH:13]=[C:14]([C:20]#[C:21][CH2:22][CH2:23][CH3:24])[CH:15]=2)[CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 123091-PentyneHCID 66111TrimethylsilylacetyleneHCID 6405952-(Benzyloxy)-6-bromonaphthalene

생성물 1

HCID 229258062-(Benzyloxy)-6-(2-n-propylethynyl)naphthalene

실험 절차

The reaction was conducted in the same manner as in the step (i) of the Example 31, except for using 2-(benzyloxy)-6-bromonaphthalene synthesized in the step (i) and 1-n-pentyne instead of 1-bromo-4-n-propylbenzene and trimethylsilylacetylene, respectively. The resultant was recrystallized from ethanol to give 2-(benzyloxy)-6-(2-n-propylethynyl)naphthalene.

후처리

  1. customThe resultant was recrystallized from ethanol

출처 및 근거

ORD 기록
ord-5f136b0ba30b4f178ad1f7d0f9a890a6
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07534547B2

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