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Ethanol → Ethyl 4-chloro-3-(trifluoromethyl)benzoate

HRID 423351
ノート
印刷プレビュー

反応式

HRID 423351 の反応式
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[C:11]([F:14])([F:13])[F:12].S(=O)(=O)(O)O.[CH2:20](O)[CH3:21]>>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:8][CH2:20][CH3:21])=[O:7])=[CH:4][C:3]=1[C:11]([F:12])([F:13])[F:14]
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

4

反応物 3

HCID 702EthanolHCID 1118Sulfuric AcidHCID 27738574-Chloro-3-(trifluoromethyl)benzoic acid

生成物 1

HCID 46311320Ethyl 4-chloro-3-(trifluoromethyl)benzoate

反応条件

温度
120 °C

実験手順

A solution of 4-chloro-3-trifluoromethyl benzoic acid (10 g, 44.5 mmol) in ethanol (10 ml) was split equally between two microwave vials. Concentrated sulfuric acid (0.75 ml) was added to each vial (1.5 ml in total). The reactions were heated in the microwave at 120° C. for 30 minutes in total. The reaction mixtures were combined and concentrated in vacuo. The residue was partitioned between EtOAc (100 ml) and aq. sodium bicarbonate (100 ml), the organic phase was separated, washed with aq. sodium bicarbonate (100 ml) and water (2×100 ml) and then dried (phase separator) and the solvent removed in vacuo to give the title compound (4.126 g) as a colourless oil. δH (400 MHz, methanol-d4) 1.40 (3H, t), 4.41 (2H, quart), 7.76 (1H, d), 8.22 (1H, dd), 8.34 (1H, d).

後処理

  1. customThe reaction mixtures
  2. concentrationconcentrated in vacuo
  3. customThe residue was partitioned between EtOAc (100 ml) and aq. sodium bicarbonate (100 ml)
  4. customthe organic phase was separated
  5. washwashed with aq. sodium bicarbonate (100 ml) and water (2×100 ml)
  6. customdried (phase separator)
  7. customthe solvent removed in vacuo

出典と根拠

ORDレコード
ord-7a28d46fbd824a79bcddfd9662b9d82c
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08101775B2

反応ノート

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