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Water → 7-Aminocarbonyl-6-chloro-2,3-dihydro-2,2-dimethylbenzofuran

HRID 1078233
ノート
印刷プレビュー

反応式

HRID 1078233 の反応式
[Cl:1][C:2]1[CH:12]=[CH:11][C:5]2[CH2:6][C:7]([CH3:10])([CH3:9])[O:8][C:4]=2[C:3]=1[C:13]#[N:14].[OH-:15].[K+].O>CC(O)(C)C>[NH2:14][C:13]([C:3]1[C:4]2[O:8][C:7]([CH3:10])([CH3:9])[CH2:6][C:5]=2[CH:11]=[CH:12][C:2]=1[Cl:1])=[O:15]
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 962WaterHCID 14797Potassium HydroxideHCID 538583176-Chloro-7-cyano-2,3-dihydro-2,2-dimethylbenzofuran

生成物 1

HCID 539852047-Aminocarbonyl-6-chloro-2,3-dihydro-2,2-dimethylbenzofuran収率 75.7%

試薬・触媒・溶媒 1

HCID 6386tert-Butanol溶媒

実験手順

A stirred solution of 10.0 grams (0.048 mole) of 6-chloro-7-cyano-2,3-dihydro-2,2-dimethylbenzofuran in 200 mL of 2-methyl-2-propanol is warmed to reflux, and 9.5 grams (0.17 mole) of 85% potassium hydroxide is added in one portion. Upon completion of addition, the reaction mixture is heated at reflux for about 75 minutes. The reaction mixture is then cooled and poured into 400 mL of water that is cooled in an ice bath. The resultant solid is collected by filtration and dried under vacuum, yielding 8.2 grams of 7-aminocarbonyl-6-chloro-2,3-dihydro-2,2-dimethylbenzofuran. The NMR spectrum is consistent with the proposed structure.

後処理

  1. temperatureto reflux
  2. additionUpon completion of addition
  3. temperaturethe reaction mixture is heated
  4. temperatureat reflux for about 75 minutes
  5. temperatureThe reaction mixture is then cooled
  6. temperatureis cooled in an ice bath
  7. filtrationThe resultant solid is collected by filtration
  8. customdried under vacuum

出典と根拠

ORDレコード
ord-3f40e392431e4822a60806e64859792d
出典データセット
uspto-grants-1996_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05547954

反応ノート

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