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Hydrochloric Acid → 1-Propioloylpyrrolidine

HRID 2191080
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HRID 2191080 반응식
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.C[C:7]#[C:8][C:9]([O-])=[O:10].Cl>O.CO.C(Cl)Cl>[C:9]([N:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1)(=[O:10])[C:8]#[CH:7]
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참가 물질

7

반응물 3

HCID 313Hydrochloric AcidHCID 31268PyrrolidineHCID 6994510HCID 6994510, 화합물

생성물 1

HCID 3378061-Propioloylpyrrolidine수율 98%

시약·촉매·용매 3

HCID 887Methanol용매HCID 962Water용매HCID 6344
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Dichloromethane
용매

실험 절차

To a stirred solution of pyrrolidine (4.2 mL, 50.0 mmol) in water (25 mL) and MeOH (35 mL) at −50° C. was added methylpropiolate (4.5 mL, 50.0 mmol) dropwise. The reaction mixture was stirred at this temperature for 5 h then diluted with DCM (200 mL). 2M aqueous HCl (200 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (2×100 mL). The combined organic layers were washed with aqueous sat. NaHCO3 (200 mL), water (200 mL), then brine (200 mL), dried (Na2SO4), filtered and concentrated in vacuo to give the title compound (6.0 g, 98%) as a white solid that was used without further purification. δH (CDCl3) 3.68 (2H, t, J 6.8 Hz), 3.50 (2H, t, J 6.3 Hz), 3.04 (1H, s), 2.01-1.90 (4H, m).

후처리

  1. customthe layers were separated
  2. extractionThe aqueous layer was extracted with DCM (2×100 mL)
  3. washThe combined organic layers were washed with aqueous sat. NaHCO3 (200 mL), water (200 mL)
  4. dry with materialbrine (200 mL), dried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-ecc256d397de4f7da88291afcae7638b
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08324204B2

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