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Hydrogen Bromide → Bis(4-hydroxyphenyl)-2,4,5-trimethylphenylphosphine oxide

HRID 1270567
ノート
印刷プレビュー

反応式

HRID 1270567 の反応式
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([P:9](=[O:27])([C:19]2[CH:24]=[CH:23][C:22]([O:25]C)=[CH:21][CH:20]=2)[C:10]2[CH:15]=[C:14]([CH3:16])[C:13]([CH3:17])=[CH:12][C:11]=2[CH3:18])=[CH:5][CH:4]=1.Br.[K+].[Br-].S([O-])([O-])=O.[Na+].[Na+].CBr>>[OH:2][C:3]1[CH:8]=[CH:7][C:6]([P:9](=[O:27])([C:19]2[CH:20]=[CH:21][C:22]([OH:25])=[CH:23][CH:24]=2)[C:10]2[CH:15]=[C:14]([CH3:16])[C:13]([CH3:17])=[CH:12][C:11]=2[CH3:18])=[CH:5][CH:4]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 5

HCID 260Hydrogen BromideHCID 6323Methyl BromideHCID 24437Sodium SulfiteHCID 253877Potassium BromideHCID 22290123Bis(4-methoxyphenyl)-2,4,5-trimethylphenylphosphine oxide

生成物 1

HCID 22290104Bis(4-hydroxyphenyl)-2,4,5-trimethylphenylphosphine oxide収率 68.9%

反応条件

温度
118 °C

実験手順

A reaction flask containing the bis(4-methoxyphenyl)-2,4,5-trimethylphenylphosphine oxide mixture (443.7 g) was charged with 48% aq. HBr (934 mL) and KBr (59.5 g). The flask was fitted with a sodium sulfite scrubber for containment of methyl bromide. The reaction mixture was heated to reflux (118° C.) and maintained at reflux until complete based on HPLC analysis. The molten product was worked up to give 283.3 g of bis(4-hydroxyphenyl)-2,4,5-trimethylphenylphosphine oxide mixture as a cream solid (68.9% yield). The ratio of products in the mixture based on 31P NMR was 39% tris(4-hydroxyphenyl)phosphine oxide, 49% bis(4-hydroxyphenyl)-2,4,5-trimethylphenylphosphine oxide, 11% di-2,4,5-trimethylphenyl-4-hydroxyphenyl-phosphine oxide, and 1% tris(2,4,5-trimethylphenyl)phosphine oxide.

後処理

  1. temperatureThe reaction mixture was heated
  2. temperaturemaintained
  3. temperatureat reflux

出典と根拠

ORDレコード
ord-51ea76901a224da78685de94564bb284
出典データセット
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07202311B2

反応ノート

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