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Water → HCID 67512779, 화합물

HRID 244375
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HRID 244375 반응식
[OH:1][C:2]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[C:4]([CH3:15])[CH:3]=1.[C:16](=O)([O-])[O-].[K+].[K+].O.C(O[CH2:27][CH3:28])(=O)C>CN(C)C=O.C1OCCOCCOCCOCCOCCOC1>[CH3:15][C:4]1[CH:3]=[C:2]([O:1][CH2:16][CH:27]=[CH2:28])[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:5]=1[C:6]([O:8][CH3:9])=[O:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 58376048Methyl 4-hydroxy-2-methyl-5-nitrobenzoate

생성물 1

HCID 67512779HCID 67512779, 화합물

시약·촉매·용매 2

HCID 2855718-Crown-6촉매
HCID 6228
Dimethylformamide
용매

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온도
80 °C

실험 절차

To a solution of methyl 4-hydroxy-2-methyl-5-nitrobenzoate (6.3 g) in N,N-dimethyl-formamide (150 ml) were added at room temperature 18-crown-6 (79 mg) and potassium carbonate (8.3 g), and the mixture was stirred at 80° C. for one hour. The mixture was cooled to room temperature, and to the reaction solution were added water and ethyl acetate, and the mixture was extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure to give the title compound (7.5 g).

후처리

  1. temperatureThe mixture was cooled to room temperature
  2. extractionthe mixture was extracted with ethyl acetate
  3. dry with materialThe organic layer was dried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-acb17f18e12e4257bed4406b09b9df21
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658639B2

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