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Carbon tetrabromide → 3-(2,2-Dibromoethenyl)-5-trimethylsilylfuran

HRID 2050647
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반응식

HRID 2050647 반응식
[CH3:1][Si:2]([CH3:11])([CH3:10])[C:3]1[O:4][CH:5]=[C:6]([CH:8]=O)[CH:7]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C:31](Br)(Br)([Br:33])[Br:32]>ClCCl>[Br:32][C:31]([Br:33])=[CH:8][C:6]1[CH:7]=[C:3]([Si:2]([CH3:11])([CH3:10])[CH3:1])[O:4][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11205Carbon tetrabromideHCID 11776TriphenylphosphineHCID 156632515-(Trimethylsilyl)furan-3-carbaldehyde2회

생성물 1

HCID 199915873-(2,2-Dibromoethenyl)-5-trimethylsilylfuran

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of 2-trimethylsilyl-4-furaldehyde (Compound 4, 1.0 g, 5.95 mmol) in dichloromethane (2 ml) was added to a solution of triphenylphosphine (3.9 g, 14.9 mmol) and carbon tetrabromide 2.46 g, 7.44 mmol) in dichloromethane (15 ml) at 0° under argon. After 1 hour, the mixture was extracted thoroughly with pentane. Evaporation of the pentane extracts gave an oil, which was flash chromatographed on silica using hexane. Fractions with Rf of about 0.52 on evaporation gave the title silylfuran as a yellow oil.

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후처리

  1. extractionthe mixture was extracted thoroughly with pentane
  2. customEvaporation of the pentane extracts
  3. customgave an oil, which
  4. customchromatographed on silica
  5. customFractions with Rf of about 0.52 on evaporation

출처 및 근거

ORD 기록
ord-e83e0ba68b2b450caa207ecec239906a
출처 데이터셋
uspto-grants-1991_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05013850

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