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

HRID 1741005
ノート
印刷プレビュー

反応式

HRID 1741005 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

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

生成物 1

HCID 222626301-(Bromomethyl)-4-(4-fluorophenoxy)benzene収率 192.4%

試薬・触媒・溶媒 2

HCID 241Benzene溶媒2 回HCID 962Water溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-8cfffd63b7194aeaa6e969296fc1cd52
出典データセット
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05972972

反応ノート

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