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Methyl Bromide → Methyl tris(p-t-amylphenyl)phosphonium Bromide

HRID 444432
ノート
印刷プレビュー

反応式

HRID 444432 の反応式
[C:1]([C:6]1[CH:11]=[CH:10][C:9]([P:12]([C:24]2[CH:29]=[CH:28][C:27]([C:30]([CH2:33][CH3:34])([CH3:32])[CH3:31])=[CH:26][CH:25]=2)[C:13]2[CH:18]=[CH:17][C:16]([C:19]([CH2:22][CH3:23])([CH3:21])[CH3:20])=[CH:15][CH:14]=2)=[CH:8][CH:7]=1)([CH2:4][CH3:5])([CH3:3])[CH3:2].[CH3:35][Br:36]>C1C=CC=CC=1>[Br-:36].[CH3:35][P+:12]([C:13]1[CH:18]=[CH:17][C:16]([C:19]([CH2:22][CH3:23])([CH3:21])[CH3:20])=[CH:15][CH:14]=1)([C:24]1[CH:29]=[CH:28][C:27]([C:30]([CH2:33][CH3:34])([CH3:31])[CH3:32])=[CH:26][CH:25]=1)[C:9]1[CH:10]=[CH:11][C:6]([C:1]([CH2:4][CH3:5])([CH3:2])[CH3:3])=[CH:7][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6323Methyl BromideHCID 12900990Tris(p-t-amylphenyl)phosphine

生成物 1

HCID 23463778Methyl tris(p-t-amylphenyl)phosphonium Bromide収率 97%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

A mixture containing 28.3 g (0.06 mole) of tris(p-t-amylphenyl)phosphine, 28.5 g (0.3 mole) of methyl bromide and 200 cc of benzene was prepared and stored at ambient temperature for 24 hours. The solvent was then removed under reduced pressure and the solid residue was stirred together with a quantity of diethyl ether for one hour. The recovered solid material weighed 33 g (97% yield) after drying and was found to contain 71.3% carbon, 8.44% hydrogen, 5.15% phosphorus and 14.0% bromine. The calculated values for the expected compound are 72.0% carbon, 8.47% hydrogen, 5.47% phosphorus and 14.1% bromine.

後処理

  1. customwas prepared
  2. customThe solvent was then removed under reduced pressure
  3. customafter drying

出典と根拠

ORDレコード
ord-be7c1c2ec12744d7918fdaef5340193e
出典データセット
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04264593

反応ノート

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