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Pyridine → 1-(Bromomethyl)-4-(4-fluorophenoxy)benzene

HRID 1741005
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HRID 1741005 반응식
[F:1][C:2]1[CH:16]=[CH:15][C:5]([O:6][C:7]2[CH:14]=[CH:13][C:10]([CH2:11]O)=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.N1C=CC=CC=1.P(Br)(Br)[Br:24]>C1C=CC=CC=1.O>[F:1][C:2]1[CH:16]=[CH:15][C:5]([O:6][C:7]2[CH:14]=[CH:13][C:10]([CH2:11][Br:24])=[CH:9][CH:8]=2)=[CH:4][CH:3]=1
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참가 물질

6

반응물 3

HCID 1049PyridineHCID 24614Phosphorus tribromideHCID 22293127[4-(4-Fluorophenoxy)phenyl]methanol

생성물 1

HCID 222626301-(Bromomethyl)-4-(4-fluorophenoxy)benzene수율 192.4%

시약·촉매·용매 2

HCID 241Benzene용매2회HCID 962Water용매

실험 절차

4-(4-Fluorophenoxy)benzyl alcohol (1.92 g, 8.80 mmol) and 0.2 ml of pyridine was dissolved in 25 ml of benzene and cooled in cold water. Phosphorus tribromide (1.19 g, 4.40 mmol) in 10 ml of benzene was added dropwise and the reaction was stirred 30 minutes and allowed to warm to room temperature. The solvent was evaporated and the residue was carefully quenched with saturated sodium bicarbonate solution. After dilution with water, the mixture was extracted twice with diethyl ether. The organic extracts were washed with saturated sodium bicarbonate solution and then with brine, dried over MgSO4, and concentrated to afford 2.38 g (96%) of the subtitle compound.

후처리

  1. customThe solvent was evaporated
  2. customthe residue was carefully quenched with saturated sodium bicarbonate solution
  3. extractionAfter dilution with water, the mixture was extracted twice with diethyl ether
  4. washThe organic extracts were washed with saturated sodium bicarbonate solution
  5. dry with materialwith brine, dried over MgSO4
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-8cfffd63b7194aeaa6e969296fc1cd52
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05972972

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