Triphenylphosphine → (3,5-Dimethoxybenzyl)triphenylphosphonium bromide

HRID 435128

反応式

HRID 435128 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([O:11][CH3:12])[CH:10]=1)[CH2:6][Br:7].[C:13]1([P:19]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C(#N)C>[Br-:7].[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([O:11][CH3:12])[CH:10]=1)[CH2:6][P+:19]([C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1)([C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1

参加物

4

反応物 2

HCID 11776TriphenylphosphineHCID 12744903,5-Dimethoxybenzyl Bromide

生成物 1

HCID 10962038(3,5-Dimethoxybenzyl)triphenylphosphonium bromide

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

The 3,5-dimethoxybenzyl triphenylphosphonium bromide is prepared by refluxing a mixture of 3,5-dimethoxybenzyl bromide (12 g.) and triphenylphosphine (14.2 g.) in acetonitrile (200 ml.) for one hour. The reaction mixture is then cooled and the crystalline product recovered by filtration, washed with ether and dried (20 g.); m.p. 269°-270° C.

後処理

  1. temperatureby refluxing
  2. temperatureThe reaction mixture is then cooled
  3. filtrationthe crystalline product recovered by filtration
  4. washwashed with ether
  5. customdried (20 g.)

出典と根拠

ORDレコード
ord-9d867849b40a402cb2a40aa7049f0b68
出典データセット
uspto-grants-1983_08
特許番号
US04400385

関連ノート

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