ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

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

HRID 1734610
ノート
印刷プレビュー

反応式

HRID 1734610 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 was warmed to reflux, and 9.5 grams (0.17 mole) of 85% potassium hydroxide was added in one portion. Upon completion of addition, the reaction mixture was heated at reflux for about 75 minutes. The reaction mixture was then cooled and poured into 400 mL of water that was cooled in an ice bath. The resultant solid was 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 was consistent with the proposed structure.

後処理

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

出典と根拠

ORDレコード
ord-f3f321cef8b24e88b6ad3424d1bcebfd
出典データセット
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05534518

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート