2-Bromopyridine → HCID 21187637, 화합물

HRID 969562노트

반응식

HRID 969562 반응식
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.C([Li])CCC.[CH2:13]1[O:23][C:16]2([CH2:21][CH2:20][C:19](=[O:22])[CH2:18][CH2:17]2)[O:15][CH2:14]1>CCOCC>[N:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[C:19]1([OH:22])[CH2:20][CH2:21][C:16]2([O:23][CH2:13][CH2:14][O:15]2)[CH2:17][CH2:18]1

참가 물질

5

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온도
0 °C

실험 절차

To a solution of 2-bromopyridine (14 g, 88.6 mmol) in anhydrous ether (300 mL) cooled at −78° C. was slowly added a solution of 2.5 M n-butyl lithium (36 mL). After the addition, stirring was continued at −78° C. for 1 hour. To it was slowly added a solution of 1,4-cyclohexanedione mono-ethylene ketal (15 g, 96 mmol) in anhydrous ether (300 mL). When the addition was complete, the mixture was allowed to warm to 0° C. and stirring was continued for 1 hour. The reaction was quenched by addition of an aqueous solution (100 mL) of ammonium chloride (4.5 g). The organic phase was separated and the aqueous phase was extracted with methylene chloride 4 times. The combined organic phases were dried over MgSO4 and concentrated. Crystallization from EtOAc provided 7 g of the desired product. The mother liquid was purified on silica gel eluting with 10% MeOH/EtOAc to give another 3 g of the desired product. MS calculated for C13H17NO3: (M+H)+236; found 236.0.

후처리

  1. additionAfter the addition
  2. additionWhen the addition
  3. stirringstirring
  4. waitwas continued for 1 hour
  5. customThe reaction was quenched by addition of an aqueous solution (100 mL) of ammonium chloride (4.5 g)
  6. customThe organic phase was separated
  7. extractionthe aqueous phase was extracted with methylene chloride 4 times
  8. dry with materialThe combined organic phases were dried over MgSO4
  9. concentrationconcentrated
  10. customCrystallization from EtOAc

출처 및 근거

ORD 기록
ord-cefe049422504858a4581852c5ecd00c
출처 데이터셋
uspto-grants-2007_12
특허 번호
US07307086B2

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