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Diketene → HCID 22028659, 화합물

HRID 1710475
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HRID 1710475 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:14]=[C:15]1[O:19][C:17](=[O:18])[CH2:16]1>CN(C=O)C>[C:17]([N:11]1[CH2:12][CH2:13][N:8]([C:6]([O:5][C:1]([CH3:4])([CH3:2])[CH3:3])=[O:7])[CH2:9][CH2:10]1)(=[O:18])[CH2:16][C:15]([CH3:14])=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12661DiketeneHCID 143452tert-Butyl piperazine-1-carboxylate

생성물 1

HCID 22028659HCID 22028659, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

1-tert-Butoxycarbonylpiperazine (103 g) was dissolved in DMF (600 mL) and diketene (56 mL) was added over 20 min at room temperature. The mixture was stirred for 2 hr. The solvent was evaporated under reduced pressure and the residue was diluted with ethyl acetate. The mixture washed with water and saturated brine and dried. The solvent was evaporated under reduced pressure to give 1-acetoacetyl-4-tert-butoxycarbonyl piperazine (129 g) as a pale-brown powder.

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custom
The solvent was evaporated under reduced pressure
  • additionthe residue was diluted with ethyl acetate
  • washThe mixture washed with water and saturated brine
  • customdried
  • customThe solvent was evaporated under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-fc384dc6a0514ad6a32722e8e5d1fe9c
    출처 데이터셋
    uspto-grants-2010_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07790725B2

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