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1-Bromopropane → HCID 86669352, 화합물

HRID 2178078
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HRID 2178078 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([N+:11]([O-:13])=[O:12])[C:9]=1[OH:10])[CH:5]=[O:6].[C:14]([O-])([O-])=O.[K+].[K+].Br[CH2:21][CH2:22][CH3:23].C(O[CH2:28][CH3:29])(=O)C>CN(C=O)C>[N+:11]([C:8]1[CH:7]=[C:4]([CH:3]=[C:2]([O:1][CH2:14][CH2:28][CH3:29])[C:9]=1[O:10][CH2:21][CH2:22][CH3:23])[CH:5]=[O:6])([O-:13])=[O:12]
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참가 물질

6

반응물 4

HCID 78401-BromopropaneHCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 57489573,4-Dihydroxy-5-nitrobenzaldehyde

생성물 1

HCID 86669352HCID 86669352, 화합물수율 32.91%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
80 °C

실험 절차

To a solution of 3,4-dihydroxy-5-nitrobenzaldehyde (400 mg, 2.185 mmol) in DMF (5 mL) was added K2CO3 (603 mg, 4.37 mmol) and 1-bromopropane (0.5 mL, excess), and the reaction was stirred at 80° C. overnight. Ethyl acetate (100 mL) was added and was washed with 2N aqueous HCl solution (20 mL×1), brine (20 mL×3), dried over Na2SO4, filtered, concentrated. The residue was purified by column chromatography (192 mg, yield: 32.91%).

후처리

  1. washwas washed with 2N aqueous HCl solution (20 mL×1), brine (20 mL×3)
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe residue was purified by column chromatography (192 mg, yield: 32.91%)

출처 및 근거

ORD 기록
ord-993af1eb9eb2404e8590475b7f62088c
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09067893B2

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