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

HRID 423316
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HRID 423316 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

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온도
100 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-248d688c36c04263bd7aa93ba0bb65da
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08101775B2

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