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Sodium Hydroxide → HCID 23081559, 화합물

HRID 884077
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HRID 884077 반응식
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH2:19][CH2:18][CH:12]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH2:11][CH2:10]2)=[CH:5][CH:4]=1.B(Br)(Br)Br.[OH-].[Na+]>ClCCl>[OH:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH2:10][CH2:11][CH:12]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH2:18][CH2:19]2)=[CH:5][CH:4]=1
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참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 25134Boron tribromideHCID 68525969HCID 68525969, 화합물

생성물 1

HCID 23081559HCID 23081559, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a solution of ethyl N-(4-methoxyphenyl)-isonipecotate (2.63 g, 10 mmol) in dichloromethane (100 mL) was added a solution of 2 M boron tribromide in dichloromethane (20 mL, 40 mmol), and the resulting solution was stirred for 0.5 hours at room temperature. The resulting reaction solution was poured into ice water, then an aqueous solution of 1 M sodium hydroxide (110 mL) was added to the solution. After stirring, the resulting solution was separated. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and evaporated under reduced pressure to thereby yield 2.43 g of the title compound.

후처리

  1. customThe resulting reaction solution
  2. stirringAfter stirring
  3. customthe resulting solution was separated
  4. washThe organic layer was washed with water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customevaporated under reduced pressure to thereby yield 2.43 g of the title compound

출처 및 근거

ORD 기록
ord-37b171d8e4ae489e8aa761bf319c8a86
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08236826B2

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