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Triethyl phosphite → HCID 86673423, 화합물

HRID 2362381
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HRID 2362381 반응식
Br[CH2:2][C:3]1[CH:8]=[C:7]([F:9])[CH:6]=[CH:5][C:4]=1[F:10].[P:11]([O:18]CC)([O:15][CH2:16][CH3:17])[O:12][CH2:13][CH3:14]>>[F:10][C:4]1[CH:5]=[CH:6][C:7]([F:9])=[CH:8][C:3]=1[CH2:2][P:11](=[O:18])([O:15][CH2:16][CH3:17])[O:12][CH2:13][CH3:14]
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참가 물질

3

반응물 2

HCID 31215Triethyl phosphiteHCID 5228302-(Bromomethyl)-1,4-difluorobenzene

생성물 1

HCID 86673423HCID 86673423, 화합물수율 93.3%

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온도
160 °C

실험 절차

A mixture of 2-(bromomethyl)-1,4-difluorobenzene (3 g, 14.49 mmol) and triethyl phosphite (7.72 ml, 43.5 mmol) was heated to 160° C. with stirring for 4 hours, cooled to ambient temperature and concentrated under high vacuum to remove most triethyl phosphite. The resulting residue was purified by column chromatography (20% to 30% EtOAc/Toluene) providing diethyl 2,5-difluorobenzylphosphonate (3.76 g, 13.52 mmol, 93% yield) as colorless oil. 1H NMR (500 MHz, DMSO-d6) δ 7.30-7.10 (m, 3H), 4.05-3.91 (m, 4H), 3.31-3.20 (m, 2H), 1.18 (t, J=7.0 Hz, 6H). MS Anal. Calcd. for [M+H]+ C11H16F2O3P: 265.2. found 265.3.

후처리

  • temperaturecooled to ambient temperature
  • concentrationconcentrated under high vacuum
  • customto remove most triethyl phosphite
  • customThe resulting residue was purified by column chromatography (20% to 30% EtOAc/Toluene)
  • 출처 및 근거

    ORD 기록
    ord-fdfc2485f1064bbfa40b6e8c66a97153
    출처 데이터셋
    uspto-grants-2014_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08691821B2

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