Potassium Carbonate → HCID 13723675、化合物

HRID 1448965ノート

反応式

HRID 1448965 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([OH:10])[C:5](=[CH:7][C:8]=1[CH3:9])[OH:6].C(=O)([O-])[O-].[K+].[K+].Br[C:18](Br)([CH3:24])[C:19]([O:21][CH2:22][CH3:23])=[O:20]>CC(C)=O>[CH3:1][C:2]1[C:8]([CH3:9])=[CH:7][C:5]2[O:6][CH:18]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH2:24][O:10][C:4]=2[CH:3]=1

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 10901348Propanoic acid, 2,2-dibromo-, ethyl esterHCID 127302874,5-Dimethylbenzene-1,2-diol

生成物 1

HCID 13723675HCID 13723675、化合物収率 319.7%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

A stirred solution of 4,5-dimethylcatechol (7.0 g.) in dry acetone (45 ml.) was heated under reflux, then potassium carbonate (5 g.) was added followed by the dropwise addition of ethyl dibromopropionate (3.5 g.). The addition procedure was repeated a further three times over 11/4 hours then the reaction was stirred under reflux for a further 33/4 hours. After cooling, the mixture was filtered, the solids washed well with acetone then the combined filtrate concentrated in vacuo. Water (35 ml.) was added, the resulting solid collected, washed with petrol then taken up in ether. The ethereal solution was washed with water, dried (Na2SO4) and evaporated in vacuo to give ethyl 6,7-dimethyl-1,4-benzodioxan-2-carboxylate (10.17 g.), m.p. 70°-71° C.

後処理

  1. temperatureunder reflux
  2. additionThe addition procedure
  3. custom4 hours
  4. temperatureunder reflux for a further 33/4 hours
  5. temperatureAfter cooling
  6. filtrationthe mixture was filtered
  7. washthe solids washed well with acetone
  8. concentrationthe combined filtrate concentrated in vacuo
  9. additionWater (35 ml.) was added
  10. customthe resulting solid collected
  11. washwashed with petrol
  12. washThe ethereal solution was washed with water
  13. dry with materialdried (Na2SO4)
  14. customevaporated in vacuo

出典と根拠

ORDレコード
ord-dd7618234cba4d3ea4d9b913834d861f
出典データセット
uspto-grants-1980_02
特許番号
US04188390

反応ノート

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