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3-Hydroxybenzyl alcohol → 3-(Chloromethyl)phenol

HRID 17873
ノート
印刷プレビュー

反応式

HRID 17873 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5]O.C(N(CC)CC)C.S(Cl)([Cl:19])=O>C1C=CC=CC=1>[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][Cl:19]
参加物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 1023-Hydroxybenzyl alcoholHCID 8471TriethylamineHCID 24386Thionyl Chloride

生成物 1

HCID 356833-(Chloromethyl)phenol収率 99%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒2 回

実験手順

3-Hydroxybenzylalcohol (5 g, 40 mmol) and triethylamine (5.2 ml, 60 mmol) were dissolved in benzene (250 ml), and thionylchloride (5.2 ml) dissolved in benzene (50 ml) was added thereto at 0° C. The brownish reacting solution was stirred at room temperature for 6 hours. When the reaction was completed, the solution was washed with brine, and the water layer was extracted with methylene chloride. The organic extract was dried over anhydrous magnesium sulfate and concentrated under a reduced pressure to obtain the title compound (5.7 g, 99%).

後処理

  1. additionwas added
  2. customat 0° C
  3. washthe solution was washed with brine
  4. extractionthe water layer was extracted with methylene chloride
  5. extractionThe organic extract
  6. dry with materialwas dried over anhydrous magnesium sulfate
  7. concentrationconcentrated under a reduced pressure

出典と根拠

ORDレコード
ord-1d9b2f92f1e840efb716f8ecf6ea906d
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07741323B2

反応ノート

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