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4-Hydroxybenzyl Alcohol → Bromocresol

HRID 25000
ノート
印刷プレビュー

反応式

HRID 25000 の反応式
P(Br)(Br)[Br:2].N1C=CC=CC=1.[OH:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16]O)=[CH:14][CH:13]=1>C1COCC1>[OH:11][C:12]1[CH:19]=[CH:18][C:15]([CH2:16][Br:2])=[CH:14][CH:13]=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

5

反応物 3

HCID 1254-Hydroxybenzyl AlcoholHCID 1049PyridineHCID 24614Phosphorus tribromide

生成物 1

HCID 41663Bromocresol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒4 回

反応条件

温度
-20 °C

実験手順

To a stirred solution of PBr3 (1.38 g, 5.0 mmol) in dry THF (2 ml) at −5° C. was added a solution of dry pyridine (0.201 ml) in dry THF (0.4 ml). A solution of 4-Hydroxybenzyl alcohol (1.89 g, 15.2 mmol) in dry THF (23 ml) was added drop wise to the reaction mixture. The reaction mixture was allowed to stand at room temperature for 18 hours, then diluted with THF and filtered through celite pad. The filtrate was evaporated, the resulting semisolid was redissolved in dry toluene (16 ml). The solution was maintained at −20° C. for 2 hours, and then filtered through celite pad to provide the title compound as a light yellow solution which was used without further purification.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. filtrationfiltered through celite pad
  2. customThe filtrate was evaporated
  3. dissolutionthe resulting semisolid was redissolved in dry toluene (16 ml)
  4. filtrationfiltered through celite pad

出典と根拠

ORDレコード
ord-7b0b35eb3ff04b7a9a9875af0715cb58
出典データセット
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06858602B2

反応ノート

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