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Phosphorus tribromide → 5-(Bromomethyl)-2-methoxybenzonitrile

HRID 1370118
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HRID 1370118 반응식
[C:1]([C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[CH2:6]O)#[N:2].P(Br)(Br)[Br:14]>ClCCl>[C:1]([C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[CH2:6][Br:14])#[N:2]
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참가 물질

4

반응물 2

HCID 24614Phosphorus tribromideHCID 229961945-(Hydroxymethyl)-2-methoxybenzonitrile

생성물 1

HCID 222736745-(Bromomethyl)-2-methoxybenzonitrile

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
0 °C

실험 절차

To a solution of 3-cyano-4-methoxybenzyl alcohol (500 mg) in dichloromethane (5 mL) was added phosphorus tribromide (0.146 mL) under ice-water cooling. The mixture was stirred at 0° C. for 3 hours and partitioned between chloroform and water. The separated organic layer was washed successively with water, an aqueous saturated sodium bicarbonate solution and brine. The organic layer was dried over magnesium sulfate and evaporated in vacuo. The residual solid was triturated with diisopropyl ether to give 3-cyano-4-methoxybenzyl bromide as an off-white solid (456.3 mg).

후처리

  1. custompartitioned between chloroform and water
  2. washThe separated organic layer was washed successively with water
  3. dry with materialThe organic layer was dried over magnesium sulfate
  4. customevaporated in vacuo
  5. customThe residual solid was triturated with diisopropyl ether

출처 및 근거

ORD 기록
ord-e86e137fd44248c0a693a50727711c04
출처 데이터셋
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06582351B1

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