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Hydrochloric Acid → 3-Methoxy-4-methylbenzyl chloride

HRID 1374994
ノート
印刷プレビュー

反応式

HRID 1374994 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[CH3:11])[CH2:6]O.[ClH:12].C(OC(C)C)(C)C>C1(C)C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[CH3:11])[CH2:6][Cl:12]
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 313Hydrochloric AcidHCID 7914Diisopropyl EtherHCID 11744818(3-Methoxy-4-methylphenyl)methanol

生成物 1

HCID 116152543-Methoxy-4-methylbenzyl chloride

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
90 °C

実験手順

A mixture of 3-methoxy-4-methylbenzylalcohol (41.61 g), conc. hydrochloric acid (125 ml) and toluene (83 ml) was stirred at 90° C. for 1 hour. After cooling, ice-water (125 ml) and diisopropyl ether (80 ml) were added to the mixture, and the organic layer was separated, and the aqueous layer was extracted with diisopropyl ether (160 ml). The combined organic layer was washed with saturated sodium hydrogen carbonate solution and brine, dried over sodium sulfate, and evaporated in vacuo to give 3-methoxy-4-methylbenzyl chloride (46.35 g) as an oil.

後処理

  1. temperatureAfter cooling
  2. customthe organic layer was separated
  3. extractionthe aqueous layer was extracted with diisopropyl ether (160 ml)
  4. washThe combined organic layer was washed with saturated sodium hydrogen carbonate solution and brine
  5. dry with materialdried over sodium sulfate
  6. customevaporated in vacuo

出典と根拠

ORDレコード
ord-39ffb9a30e824374a9106730e09699e4
出典データセット
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07166598B2

反応ノート

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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