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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Chloroethyl chloroformate → 4-(2-Chlorophenyl)-4-methylpiperidine

HRID 242618
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HRID 242618 반응식
C([N:8]1[CH2:13][CH2:12][C:11]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[Cl:21])([CH3:14])[CH2:10][CH2:9]1)C1C=CC=CC=1.ClC(OC(Cl)C)=O>ClCCCl>[Cl:21][C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[C:11]1([CH3:14])[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]1
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참가 물질

4

반응물 2

HCID 5213051-Chloroethyl chloroformateHCID 23136891HCID 23136891, 화합물

생성물 1

HCID 231369824-(2-Chlorophenyl)-4-methylpiperidine수율 73.4%

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

A solution of 1-benzyl-4-(2-chloro-phenyl)-4-methyl-piperidine (0.59 g, 1.95 mmol) in 1,2-dichloroethane (10 mL) was treated with 1-chloroethyl chloroformate (0.28 mL, 2.6 mmol). This mixture was stirred for 12 hr at reflux, then evaporated in vacuo. The residue was redissolved in methanol (10 mL) and heated to reflux for 1 hr, then evaporated in vacuo. The resulting brown solid (the hydrochloric salt) was washed with ethyl acetate, then freebased with ethyl acetate/sodium hydroxide to yield 0.30 g (72%) of the title compound, ESI-MS m/z: 246 [M+1].

후처리

  1. temperatureat reflux
  2. customevaporated in vacuo
  3. dissolutionThe residue was redissolved in methanol (10 mL)
  4. temperatureheated
  5. temperatureto reflux for 1 hr
  6. customevaporated in vacuo
  7. washThe resulting brown solid (the hydrochloric salt) was washed with ethyl acetate

출처 및 근거

ORD 기록
ord-a073c4344ab843f69cdfb4ed56986d72
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08653096B2

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