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2-(5-chloro-2-nitrophenylmethyl)benzoic Acid Methyl Ester → 2-(2-amino-5-chlorophenylmethyl)benzoic Acid Methyl Ester

HRID 50144
ノート
印刷プレビュー

反応式

HRID 50144 の反応式
[CH3:1][O:2][C:3](=[O:21])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[CH2:10][C:11]1[CH:16]=[C:15]([Cl:17])[CH:14]=[CH:13][C:12]=1[N+:18]([O-])=O>C(O)(=O)C.O>[CH3:1][O:2][C:3](=[O:21])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[CH2:10][C:11]1[CH:16]=[C:15]([Cl:17])[CH:14]=[CH:13][C:12]=1[NH2:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 213015592-(5-chloro-2-nitrophenylmethyl)benzoic Acid Methyl Ester

生成物 1

HCID 120966522-(2-amino-5-chlorophenylmethyl)benzoic Acid Methyl Ester収率 47.9%

試薬・触媒・溶媒 1

HCID 21899381Acetic acid--water (1/1)溶媒

実験手順

To a solution of 2-(2-nitro-5-chlorophenylmethyl) benzoic acid methyl ester (840 mg; prepared in reference example 3) in a mixture of acetic acid-water (5:1; 12 ml) was added steel powder (768 mg) and the mixture was added for 20 minutes at 80° C. The suspension was poured into ice-water and was extracted with ethyl acetate. The organic layer was washed with water, a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride successively, dried, and was concentrated. The residue was purified by column chromatography on silica gel to give the title compound (363 mg) having the following physical data.

後処理

  1. additionthe mixture was added for 20 minutes at 80° C
  2. extractionwas extracted with ethyl acetate
  3. washThe organic layer was washed with water
  4. dry with materiala saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride successively, dried
  5. concentrationwas concentrated
  6. customThe residue was purified by column chromatography on silica gel

出典と根拠

ORDレコード
ord-694ae5d4bfeb4d09a7f47bf569145a22
出典データセット
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06710205B2

反応ノート

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