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2-Benzofurancarboxaldehyde → 2-Vinylbenzofuran

HRID 1459660
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인쇄 미리보기

반응식

HRID 1459660 반응식
[CH3:1]C(C)([O-])C.[K+].[O:7]1[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[CH:9]=[C:8]1[CH:16]=O>O1CCCC1.[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.CN(C)C=O>[CH:16]([C:8]1[O:7][C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[CH:9]=1)=[CH2:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 613412-BenzofurancarboxaldehydeHCID 23665647Potassium tert-butoxide

생성물 1

HCID 5889742-Vinylbenzofuran

시약·촉매·용매 3

HCID 74505Methyltriphenyliphosphonium bromide촉매HCID 6228Dimethylformamide용매HCID 8028Tetrahydrofuran용매2회

실험 절차

92 ml of a 1N solution of potassium tert-butoxide in tetrahydrofuran are added dropwise to a vigorously stirred mixture at 0° C. of 68.4 mmol of benzofuran-2-carboxaldehyde and 92 mmol of methyltriphenylphosphonium bromide in 200 ml of tetrahydrofuran and 150 ml of dimethylformamide. The medium is stirred for 2 h at room temperature, poured into 2 liters of ice-water and extracted with ether. After concentration of the solvents, the residue is taken up in 1 liter of petroleum ether and the precipitate is filtered off and washed with petroleum ether. The expected product is obtained by evaporation of the filtrate.

후처리

  1. extractionextracted with ether
  2. filtrationthe precipitate is filtered off
  3. washwashed with petroleum ether

출처 및 근거

ORD 기록
ord-abc4f898b19744728300d93751798b6c
출처 데이터셋
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05854273

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