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Sodium hydride → 1-(Trifluoromethyl)-3-(4-vinylphenoxy)benzene

HRID 705827
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인쇄 미리보기

반응식

HRID 705827 반응식
[H-].[Na+].[F:3][C:4]([F:21])([F:20])[C:5]1[CH:6]=[C:7]([CH:17]=[CH:18][CH:19]=1)[O:8][C:9]1[CH:16]=[CH:15][C:12]([CH:13]=O)=[CH:11][CH:10]=1.[I-].[CH3:23][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>C1COCC1>[F:3][C:4]([F:21])([F:20])[C:5]1[CH:19]=[CH:18][CH:17]=[C:7]([O:8][C:9]2[CH:16]=[CH:15][C:12]([CH:13]=[CH2:23])=[CH:11][CH:10]=2)[CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 638159Methyltriphenylphosphonium iodideHCID 121487884-(3-(Trifluoromethyl)phenoxy)benzaldehyde

생성물 1

HCID 677746121-(Trifluoromethyl)-3-(4-vinylphenoxy)benzene수율 98.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

NaH (23.66 g, 592 mmol) was added to the solution of 4-(3-(trifluoromethyl)phenoxy)-benzaldehyde (25 g, 94 mmol) and methyltriphenylphosphonium iodide (36.2 g, 101 mmol) in THF (180 mL) at 0° C. The reaction mixture was stirred at room temperature overnight. Purification via a flash column chromatography then afforded the title compound as a colorless oil (24.4 g, 98% yield).

후처리

  1. customPurification via a flash column chromatography

출처 및 근거

ORD 기록
ord-14373879cdff4a638e3d21e60aa5b6dd
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09174968B2

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