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Water → Methyl 2-amino-4-(2-chloroethoxy)-5-methoxybenzoate

HRID 612031
ノート
印刷プレビュー

反応式

HRID 612031 の反応式
[CH3:1][O:2][C:3](=[O:19])[C:4]1[CH:9]=[C:8]([O:10][CH3:11])[C:7]([O:12][CH2:13][CH2:14][Cl:15])=[CH:6][C:5]=1[N+:16]([O-])=O.[Cl-].[NH4+].O>[Fe].CO>[CH3:1][O:2][C:3](=[O:19])[C:4]1[CH:9]=[C:8]([O:10][CH3:11])[C:7]([O:12][CH2:13][CH2:14][Cl:15])=[CH:6][C:5]=1[NH2:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 962WaterHCID 25517Ammonium ChlorideHCID 23032998Methyl 4-(2-chloroethoxy)-5-methoxy-2-nitrobenzoate

生成物 1

HCID 23033001Methyl 2-amino-4-(2-chloroethoxy)-5-methoxybenzoate

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 887Methanol溶媒

実験手順

A mixture of 68.2 g (235.4 mmol) of 4-(2-chloro-ethoxy)-5-methoxy-2-nitro-benzoic acid methyl ester and 52.6 g (941.8 mmol) of iron was mechanically stirred at reflux in a mixture containing 62.9 g ammonium chloride, 393 ml water, and 1021 ml methanol for 15 hr. The mixture was concentrated and mixed with ethyl acetate. The organic solution was washed with water and saturated sodium bicarbonate. The solution was dried over magnesium sulfate and filtered through a short column of silica gel. The solution was concentrated to 200 ml and diluted with 250 of hot hexane. After standing 47.7 g of the tide compound was obtained as a solid: mass spectrum (electrospray, m/e) M+H 259.8.

後処理

  1. temperatureat reflux in a mixture
  2. concentrationThe mixture was concentrated
  3. additionmixed with ethyl acetate
  4. washThe organic solution was washed with water and saturated sodium bicarbonate
  5. dry with materialThe solution was dried over magnesium sulfate
  6. filtrationfiltered through a short column of silica gel
  7. concentrationThe solution was concentrated to 200 ml
  8. additiondiluted with 250 of hot hexane
  9. customwas obtained as a solid

出典と根拠

ORDレコード
ord-1942ddee23b8431584402a4677f4fea8
出典データセット
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06002008

反応ノート

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