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Ethyl Acetate → Diethyl 1-(bromoacetyl)-2,2-pyrrolidinedicarboxylate

HRID 2245425
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HRID 2245425 반응식
[NH:1]1[CH2:5][CH2:4][CH2:3][C:2]1([C:11]([O:13][CH2:14][CH3:15])=[O:12])[C:6]([O:8][CH2:9][CH3:10])=[O:7].C(=O)([O-])[O-].[K+].[K+].[Br:22][CH2:23][C:24](Br)=[O:25].C(OCC)(=O)C>ClCCl.O>[Br:22][CH2:23][C:24]([N:1]1[CH2:5][CH2:4][CH2:3][C:2]1([C:11]([O:13][CH2:14][CH3:15])=[O:12])[C:6]([O:8][CH2:9][CH3:10])=[O:7])=[O:25]
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참가 물질

7

반응물 4

HCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 61147Bromoacetyl bromideHCID 12524347Diethyl 2,2-pyrrolidinedicarboxylate

생성물 1

HCID 59215802Diethyl 1-(bromoacetyl)-2,2-pyrrolidinedicarboxylate

시약·촉매·용매 2

HCID 962Water용매
HCID 6344
Dichloromethane
용매

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온도
0 °C

실험 절차

To a solution of diethyl 2,2-pyrrolidinedicarboxylate (D63, 900 mg) in dichloromethane (9 mL) at 0° C., potassium carbonate (0.5M solution, 12.5 mL) and bromoacetyl bromide (0.55 mL) were added. The resulting mixture was stirred at 0° C. for 2 hours. The mixture was then diluted with water and then allowed to reach r.t. Ethyl acetate (15 mL) was added and phases were separated. The aqueous phase was then extracted with ethyl acetate (2×10 mL) and washed with brine (20 mL). The organic phase was dried and concentrated in vacuo to give the desired compound (1.06 g) as orange oil.

후처리

  1. customto reach r.t
  2. customphases were separated
  3. extractionThe aqueous phase was then extracted with ethyl acetate (2×10 mL)
  4. washwashed with brine (20 mL)
  5. customThe organic phase was dried
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-92d64b0384ac40d1bc2b21aa2cb722e0
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07683056B2

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