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Hydrochloric Acid → 1-Methyl-1-(6-trifluoromethyl-pyridin-3-yl)-ethylamine hydrochloride

HRID 1672524
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HRID 1672524 반응식
[CH3:1][C:2]([NH2:14])([C:4]1[CH:5]=[N:6][C:7]([C:10]([F:13])([F:12])[F:11])=[CH:8][CH:9]=1)[CH3:3].[ClH:15]>CC(C)=O>[ClH:15].[CH3:3][C:2]([NH2:14])([C:4]1[CH:5]=[N:6][C:7]([C:10]([F:12])([F:13])[F:11])=[CH:8][CH:9]=1)[CH3:1]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 545799022-(6-(Trifluoromethyl)pyridin-3-yl)propan-2-amine

생성물 1

HCID 545799011-Methyl-1-(6-trifluoromethyl-pyridin-3-yl)-ethylamine hydrochloride수율 62%

시약·촉매·용매 1

HCID 180Acetone용매

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온도
0 °C

실험 절차

Dissolve 1-methyl-1-(6-trifluoromethyl-pyridin-3-yl)-ethylamine from Preparation F (1.0 g, 4.9 mmol) in acetone (10 mL) at ambient temperature and stir for 5 minutes. Add concentrated (12.18 N) hydrochloric acid (0.4 mL, 4.9 mmol) drop-wise with continued stirring, and observe the formation of a white solid. Cool the reaction mixture to 0° C. and continue stirring for 30 minutes. Filter the resultant solid and rinse with cold acetone (2 mL). Dry under vacuum at 40° C. to provide the titled compound (0.73 g, 62%) as a white solid: 1H NMR (400 MHz, DMSO-d6) δ 9.17 (s (br), 3H), 9.02 (d, 1H, J=2.4 Hz), 8.32 (dd, 1H, J=8.0, 2.0 Hz), 7.97 (d, 1H, J=8.4 Hz), 1.71 (s, 6H); 13C NMR (100 MHz, DMSO-d6) δ 148.0, 146.2 (q, JCF=34.0 Hz), 142.4 (d, JCF=0.8 Hz), 136.0, 121.9 (q, JCF=273 Hz), 120.8 (t, JCF=2.6 Hz), 54.9, 27.5.

후처리

  1. additionAdd
  2. stirringcontinue stirring for 30 minutes
  3. filtrationFilter the resultant solid
  4. washrinse with cold acetone (2 mL)
  5. customDry under vacuum at 40° C.

출처 및 근거

ORD 기록
ord-f84c36f05bbb4330a712c163686c3fc8
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07998985B2

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