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Methyl chloroformate → Dimethyl 2-(3,5-difluoro-4-(trifluoromethyl)phenyl)-piperidine-1,4-dicarboxylate

HRID 1963213
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HRID 1963213 반응식
Cl.[F:2][C:3]1[CH:4]=[C:5]([CH:14]2[CH2:19][CH:18]([C:20]([O:22][CH3:23])=[O:21])[CH2:17][CH2:16][NH:15]2)[CH:6]=[C:7]([F:13])[C:8]=1[C:9]([F:12])([F:11])[F:10].CCN(C(C)C)C(C)C.[C:33](Cl)(=[O:36])[O:34][CH3:35]>C(Cl)Cl>[F:13][C:7]1[CH:6]=[C:5]([CH:14]2[CH2:19][CH:18]([C:20]([O:22][CH3:23])=[O:21])[CH2:17][CH2:16][N:15]2[C:33]([O:34][CH3:35])=[O:36])[CH:4]=[C:3]([F:2])[C:8]=1[C:9]([F:12])([F:10])[F:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6586Methyl chloroformate2회HCID 81531DiisopropylethylamineHCID 86646600Methyl 2-(3,5-difluoro-4-(trifluoromethyl)phenyl)piperidine-4-carboxylate hydrochloride

생성물 1

HCID 66732303Dimethyl 2-(3,5-difluoro-4-(trifluoromethyl)phenyl)-piperidine-1,4-dicarboxylate수율 86.2%

시약·촉매·용매 1

HCID 6344Dichloromethane
용매
2회

실험 절차

Methyl 2-(3,5-difluoro-4-(trifluoromethyl)phenyl)piperidine-4-carboxylate hydrochloride (3.118 g, 8.67 mmol) and DIPEA (3.02 mL, 17.34 mmol) were dissolved in DCM (30 mL). Methyl carbonochloridate (1.024 mL, 13.00 mmol) was added and the reaction stirred at room temperature for 1.5 h. Additional methyl carbonochloridate (0.341 mL, 4.33 mmol) was added and stirring continued for 0.5 h. DCM (170 mL) was added. The organic phase was washed with 0.1 M HCl (2×200 mL), satd NaHCO3 (200 mL), dried with a phase separator and evaporated in vacuo to yield dimethyl 2-(3,5-difluoro-4-(trifluoromethyl)phenyl)-piperidine-1,4-dicarboxylate (2.85 g, 86%) as a colorless oil. MS m/z 382 (M+H)+

후처리

  1. stirringstirring
  2. waitcontinued for 0.5 h
  3. washThe organic phase was washed with 0.1 M HCl (2×200 mL), satd NaHCO3 (200 mL)
  4. customdried with a phase separator
  5. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-1c1bcb9cea864b1695afcd8a1eca6aa0
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08415378B2

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