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Trifluoroacetic acid → 4-[2-(Methylsulfanyl)phenyl]piperidine

HRID 2256048
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HRID 2256048 반응식
C(OC([N:11]1[CH2:16][CH2:15][CH:14]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[S:23][CH3:24])[CH2:13][CH2:12]1)=O)C1C=CC=CC=1.C1(SC)C=CC=CC=1.FC(F)(F)C(O)=O>>[CH3:24][S:23][C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=1[CH:14]1[CH2:15][CH2:16][NH:11][CH2:12][CH2:13]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6422Trifluoroacetic acidHCID 7520ThioanisoleHCID 111106201-Benzyloxycarbonyl-4(2-methylthiophenyl)piperidine

생성물 1

HCID 190291654-[2-(Methylsulfanyl)phenyl]piperidine수율 63%

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온도
60 °C

실험 절차

A mixture of 1-benzyloxycarbonyl-4-(2-methylthiophenyl)piperidine (0.34 g) and thioanisole (0.58 mL) was treated with trifluoroacetic acid (5 mL) and the mixture was heated to 60° C. for 30 minutes. At the end of this period, the reaction mixture was evaporated and diluted with ether. Extraction with water, neutralization of the aqueous layer with sodium bicarbonate and extraction with ethyl acetate afforded the crude product. This material was purified by column chromatography; elution with 19:1 dichloromethane:methanol containing 5% triethylamine afforded the named product (0.13 g); MS: 208 (M+1): NMR: 1.4-1.8 (q, d, J1 =25, J2 =12, 2), 1.8-1.9 (m, 2), 2.46 (s, 3), 2.8-2.9 (d, t, J1 =12, J2 =2.7, 2), 3.1-3.2 (m, 1), 3.3 (br, 2), 4.0 (br, 1), 7.1-7.3 (m, 4).

후처리

  1. customAt the end of this period, the reaction mixture was evaporated
  2. additiondiluted with ether
  3. extractionExtraction with water, neutralization of the aqueous layer
  4. extractionwith sodium bicarbonate and extraction with ethyl acetate
  5. customafforded the crude product
  6. customThis material was purified by column chromatography
  7. washelution with 19:1 dichloromethane

출처 및 근거

ORD 기록
ord-5694831843f54c1393b287ddad6a7c33
출처 데이터셋
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05654299

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