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

HRID 423351
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HRID 423351 반응식
[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]
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참가 물질

4

반응물 3

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

생성물 1

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

반응 조건

온도
120 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-7a28d46fbd824a79bcddfd9662b9d82c
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08101775B2

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