Methyl 2,6-dinitrobenzoate → Methyl 2,6-diaminobenzoate

HRID 1278434

反応式

HRID 1278434 の反応式
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]([N+:14]([O-])=O)[C:5]=1[C:6]([O:8][CH3:9])=[O:7])([O-])=O>CO.[Pd].C(Cl)(Cl)Cl>[NH2:1][C:4]1[CH:13]=[CH:12][CH:11]=[C:10]([NH2:14])[C:5]=1[C:6]([O:8][CH3:9])=[O:7]

参加物

5

反応物 1

HCID 333850Methyl 2,6-dinitrobenzoate

生成物 1

HCID 12402975Methyl 2,6-diaminobenzoate収率 96%

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 887Methanol溶媒2 回HCID 6212Chloroform溶媒

実験手順

Methyl 2,6-dinitrobenzoate (15.0 gm.) is suspended in methanol (500 ml.) and 5% palladium on charcoal (1.5 gm.) added. Reduction is carried out on a Parr apparatus for two hours. The solution is filtered with suction and the catalyst washed with a few ml. of methanol. Removal of the methanol gives a brown crystalline product. Extraction with chloroform (50 ml.) and treatment with Darco® gives the product (10.9 gm. 96% yield, m.p. 78°-79.5°). The thin layer chromatogram (Silica gel, 3% methanol in chloroform) shows the material to be homogeneous.

後処理

  1. filtrationThe solution is filtered with suction
  2. washthe catalyst washed with a few ml
  3. customRemoval of the methanol
  4. customgives a brown crystalline product
  5. extractionExtraction with chloroform (50 ml.) and treatment with Darco®
  6. customgives the product (10.9 gm. 96% yield, m.p. 78°-79.5°)

出典と根拠

ORDレコード
ord-26c51facfafb4bcd989582344b43693a
出典データセット
uspto-grants-1981_07
特許番号
US04281151

関連ノート

読み込み中…