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Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1) → HCID 67592430, 화합물

HRID 1779990
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HRID 1779990 반응식
[CH2:1]([CH:3]1[NH:7][C:6](=O)[CH2:5][CH:4]1[CH3:9])C.F[B-](F)(F)F.[CH3:15][O+:16]([CH3:18])C>C(Cl)Cl>[NH:7]([CH:3]1[CH:1]=[C:15]([O:16][CH3:18])[CH2:5][CH:4]1[CH3:9])[CH3:6]
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참가 물질

4

반응물 2

HCID 2735153Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 184286185-Ethyl-4-methyl-2-pyrrolidinone

생성물 1

HCID 67592430HCID 67592430, 화합물수율 79.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 0.254 g (2 mmol) of 5-ethyl-4-methyl-2-pyrrolidone (from step B) in 3 mL of CH2Cl2 was added 0.355 g (2.4 mmol) of trimethyloxonium tetrafluoroborate under a N2 atmosphere. After stirring overnight the reaction mixture was quenched with saturated K2CO3 solution and diluted with Et2O. The solution was filtered and the filtrate was concentrated. The residue was purified by flash chromatography using Et2O-hexane to isolate 0.224 g (79%) of the title compound.

후처리

  1. customwas quenched with saturated K2CO3 solution
  2. additiondiluted with Et2O
  3. filtrationThe solution was filtered
  4. concentrationthe filtrate was concentrated
  5. customThe residue was purified by flash chromatography

출처 및 근거

ORD 기록
ord-f48a6e7dc22546ea8439a5549e0809a6
출처 데이터셋
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05629322

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