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Ammonia → 4-(Trifluoromethyl)cyclohexane-1-carboxamide

HRID 2304906
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인쇄 미리보기

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HRID 2304906 반응식
C[N:2](C)CCCN=C=NCC.[F:12][C:13]([F:24])([F:23])[CH:14]1[CH2:19][CH2:18][CH:17]([C:20](O)=[O:21])[CH2:16][CH2:15]1.ON1C2C=CC=CC=2N=N1.N>CN(C=O)C.C(Cl)Cl.CO.C(OCC)(=O)C>[F:12][C:13]([F:24])([F:23])[CH:14]1[CH2:19][CH2:18][CH:17]([C:20]([NH2:2])=[O:21])[CH2:16][CH2:15]1
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참가 물질

9

반응물 4

HCID 222AmmoniaHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 27791824-(Trifluoromethyl)cyclohexanecarboxylic acid

생성물 1

HCID 219912124-(Trifluoromethyl)cyclohexane-1-carboxamide수율 66.7%

시약·촉매·용매 4

HCID 887
Methanol
용매
HCID 6228Dimethylformamide용매
HCID 6344Dichloromethane용매
HCID 8857Ethyl Acetate용매

반응 조건

온도
0 °C

실험 절차

At 0° C. 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (2.90 g, 15.29 mmol) was added to a solution of 4-(trifluoromethyl)cyclohexanecarboxylic acid (3.0 g, 15.29 mmol) and 1-hydroxybenzotriazole (2.1 g, 15.29 mmol) in DMF (10 ml) and DCM (10 ml). The reaction mixture was stirred for 20 min at 0° C. A saturated solution of ammonia in methanol (17 ml) was added. The reaction mixture was stirred for 16 hours, while it was warming up to room temperature. It was diluted with ethyl acetate (100 ml) and washed with a 10% aqueous solution of sodium hydrogen sulphate (100 ml). The aqueous phase was extracted with ethyl acetate (2×80 ml). The combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate (100 ml) and dried over magnesium sulphate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica, using DCM/methanol/25% aqueous ammonia (100:10:1) as eluent, to give 1.99 g of 4-trifluoromethylcyclohexanecarboxylic acid amide.

후처리

  1. customAt 0° C
  2. stirringThe reaction mixture was stirred for 16 hours, while it
  3. temperaturewas warming up to room temperature
  4. washwashed with a 10% aqueous solution of sodium hydrogen sulphate (100 ml)
  5. extractionThe aqueous phase was extracted with ethyl acetate (2×80 ml)
  6. washThe combined organic layers were washed with a saturated aqueous solution of sodium hydrogen carbonate (100 ml)
  7. dry with materialdried over magnesium sulphate
  8. customThe solvent was removed in vacuo
  9. customThe crude product was purified by flash chromatography on silica

출처 및 근거

ORD 기록
ord-63f5df730bd24654ac07ce397f7be092
출처 데이터셋
uspto-grants-2002_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06437147B1

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