1-Pyrrolidinecarboxylic acid, 2-oxo-, 1,1-dimethylethyl ester → tert-butyl N-[4-(3-fluorophenyl)-4-oxobutyl]carbamate

HRID 537768

반응식

HRID 537768 반응식
[O:1]=[C:2]1[CH2:6][CH2:5][CH2:4][N:3]1[C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8].[F:14][C:15]1[CH:16]=[C:17]([Mg]Br)[CH:18]=[CH:19][CH:20]=1>C1COCC1>[F:14][C:15]1[CH:20]=[C:19]([C:2](=[O:1])[CH2:6][CH2:5][CH2:4][NH:3][C:7](=[O:8])[O:9][C:10]([CH3:13])([CH3:12])[CH3:11])[CH:18]=[CH:17][CH:16]=1

참가 물질

4

반응 조건

온도
-78 °C

실험 절차

In a round-bottomed flask was charged tert-butyl 2-oxopyrrolidine-1-carboxylate (2.2 g, 11.9 mmol) and THF (25 mL). The mixture was cooled down to −78° C. first, followed by slow addition of (3-fluorophenyl)magnesium bromide (17.8 mL, 17.8 mmol, 1.0 M solution in THF) over 15 minutes. The mixture was stirred for 3 hours, during which time the bath temperature rose from −78° C. to −10° C. The reaction was quenched by drop-wise addition of 1N HCl (2 mL) and warmed up to ambient temperature, followed by addition of EtOAc and water. After separating the organic layer, the aqueous layer was extracted with EtOAc three times. The combined organic layers was dried over Na2SO4 and concentrated to yield the product as a clear oil.

후처리

  1. customrose from −78° C. to −10° C
  2. customThe reaction was quenched by drop-wise addition of 1N HCl (2 mL)
  3. temperaturewarmed up to ambient temperature
  4. additionfollowed by addition of EtOAc and water
  5. customAfter separating the organic layer
  6. extractionthe aqueous layer was extracted with EtOAc three times
  7. dry with materialThe combined organic layers was dried over Na2SO4
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-274f67140ff64dffb426ac3f96e73c7b
출처 데이터셋
uspto-grants-2014_10
특허 번호
US08865698B2

연결된 노트

불러오는 중…