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Dimethyl Sulfate → Ethyl 4-amino-5-cyano-2-methoxybenzoate

HRID 345579
ノート
印刷プレビュー

反応式

HRID 345579 の反応式
[NH2:1][C:2]1[C:12]([C:13]#[N:14])=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[C:4]([OH:15])[CH:3]=1.S(OC)(O[CH3:20])(=O)=O.C(=O)([O-])[O-].[K+].[K+]>CC(=O)C>[NH2:1][C:2]1[C:12]([C:13]#[N:14])=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[C:4]([O:15][CH3:20])[CH:3]=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 3

HCID 6497Dimethyl SulfateHCID 11430Potassium CarbonateHCID 3018374Ethyl 4-amino-5-cyano-2-hydroxybenzoate

生成物 1

HCID 15096747Ethyl 4-amino-5-cyano-2-methoxybenzoate収率 79.5%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

To a stirred solution of 4.1 parts of ethyl 4-amino-5-cyano-2-hydroxybenzoate in 40 parts of 2-propanone were added successively 2.52 parts of dimethyl sulfate and 4.1 parts of potassium carbonate. The whole was stirred and refluxed for 3 hours. The reaction mixture was filtered while hot and the filter-cake was washed with 2-propanone. The filtrate was evaporated and the solid residue was crystallized from 24 parts of 2-propanol, yielding 3.5 parts (79.5%) of ethyl 4-amino-5-cyano-2-methoxybenzoate; mp. 164.5° C. (intermediate 110).

後処理

  1. temperaturerefluxed for 3 hours
  2. filtrationThe reaction mixture was filtered while hot and the filter-cake
  3. washwas washed with 2-propanone
  4. customThe filtrate was evaporated
  5. customthe solid residue was crystallized from 24 parts of 2-propanol

出典と根拠

ORDレコード
ord-2069236e26d64356823bc520280143e3
出典データセット
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05057525

反応ノート

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