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2,3,4-Trimethoxy-6-nitrobenzaldehyde → HCID 21891651, 화합물

HRID 720325
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HRID 720325 반응식
[N+:1]([C:4]1[C:9]([CH:10]=[O:11])=[C:8]([O:12][CH3:13])[C:7]([O:14][CH3:15])=[C:6]([O:16][CH3:17])[CH:5]=1)([O-])=O>CO.C1COCC1.[Pd]>[NH2:1][C:4]1[C:9]([CH:10]=[O:11])=[C:8]([O:12][CH3:13])[C:7]([O:14][CH3:15])=[C:6]([O:16][CH3:17])[CH:5]=1
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참가 물질

5

반응물 1

HCID 123200312,3,4-Trimethoxy-6-nitrobenzaldehyde

생성물 1

HCID 21891651HCID 21891651, 화합물수율 88.5%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

6-Nitro-2,3,4-trimethoxybenzaldehyde (4.0 g) was dissolved in methanol (40 mL) and THF (20 mL), 10% palladium on carbon was added to the solution, and the mixture was stirred at room temperature for 5 hours under a hydrogen atmosphere. After the catalyst was removed by filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:4 to 1:3) to obtain 6-amino-2,3,4-trimethoxybenzaldehyde (3.1 g). This product was immediately dissolved in dichloromethane (35 mL), and triethylamine (4.2 mL) was added thereto. Chloroacetyl chloride (1.78 mL) was added dropwise under ice cooling, and the mixture was stirred overnight at room temperature. The reaction mixture was extracted with chloroform, and the extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. After concentrating the extract under reduced pressure, the residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:4 to 1:3) to obtain the title compound.

후처리

  1. customAfter the catalyst was removed by filtration
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. customthe residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:4 to 1:3)

출처 및 근거

ORD 기록
ord-a0518e23b87c4f709f57bcc49fbb00d1
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07135473B2

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