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Triethyl phosphite → Diethyl 3-Bromobenzylphosphonate

HRID 657394
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HRID 657394 반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8]Br)[CH:3]=1.[P:10]([O:17]CC)([O:14][CH2:15][CH3:16])[O:11][CH2:12][CH3:13].P([O-])([O-])[O-]>>[CH2:12]([O:11][P:10]([CH2:8][C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([Br:1])[CH:3]=1)(=[O:17])[O:14][CH2:15][CH3:16])[CH3:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 31215Triethyl phosphiteHCID 699793-Bromobenzyl bromideHCID 107908Phosphite

생성물 1

HCID 10979718Diethyl 3-Bromobenzylphosphonate수율 98.3%

반응 조건

온도
130 °C

실험 절차

To 1-bromo-3-(bromomethyl)benzene (100 g, 400 mmol) in a 500 mL round-bottom flask under nitrogen was added triethyl phosphite (69.6 mL, 400 mmol) and the solution was heated to 130° C. The apparatus was set up ready for distillation. As the heating block reached 130° C. the mixture began to reflux and a large volume of colourless liquid was allowed to distil off. Analysis of the reaction by hplc after 40 min showed some starting material so another 0.5 eq of the phosphite was added and heating with distillation continued. The reaction was then heated under vacuum: the excess phosphite was distilled off under vacuum (130° C. heater and 15 mbar, gradually going down to 0.5 mbar). This gave a colorless oil 120.8 g. HPLC 2.20 min (ret time), 97%; LC-MS m/z 307, 309 (M+H)+, 1.01 min (ret time).

후처리

  1. distillationThe apparatus was set up ready for distillation
  2. customreached 130° C.
  3. temperatureto reflux
  4. customto distil off
  5. customAnalysis of the reaction by hplc after 40 min
  6. additionwas added
  7. temperatureheating with distillation
  8. temperatureThe reaction was then heated under vacuum
  9. distillationthe excess phosphite was distilled off under vacuum (130° C. heater and 15 mbar

출처 및 근거

ORD 기록
ord-985ebbba984a4dd4836869a5fae14324
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08071588B2

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