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2,3,4-Trimethoxy-6-nitrobenzaldehyde → HCID 21891651、化合物

HRID 720325
ノート
印刷プレビュー

反応式

HRID 720325 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 1

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

生成物 1

HCID 21891651HCID 21891651、化合物収率 88.5%

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-a0518e23b87c4f709f57bcc49fbb00d1
出典データセット
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07135473B2

反応ノート

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