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

HRID 423316
ノート
印刷プレビュー

反応式

HRID 423316 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
100 °C

実験手順

4-Chloro-3-(trifluoromethyl)benzoic acid (1 g, 4.45 mmol) was dissolved in ethanol (3 ml) and concentrated sulfuric acid (0.15 ml) was added. The mixture was heated in the microwave at 100° C. for 5 minutes and then 120° C. for 15 minutes. The solvent was removed in vacuo and the residue partitioned between saturated aq. sodium bicarbonate (50 ml) and ethyl acetate (50 ml). The aqueous layer was extracted with further EtOAc (50 ml) and the organic phases were combined, dried with a phase separator and concentrated in vacuo to give the title compound (1.026 g) (DN108121-148A3) as a colourless oil. δH (methanol-d4, 400 MHz) 1.40 (3H, t), 4.41 (2H, q), 7.76 (1H, d), 8.21 (1H, dd), 8.33 (1H, d). MS (ES) no mass ion observed.

後処理

  1. customThe solvent was removed in vacuo
  2. customthe residue partitioned between saturated aq. sodium bicarbonate (50 ml) and ethyl acetate (50 ml)
  3. extractionThe aqueous layer was extracted with further EtOAc (50 ml)
  4. customdried with a phase separator
  5. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-248d688c36c04263bd7aa93ba0bb65da
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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