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

Hydrochloric Acid → 1,4-Bis[4-[(1-benzyloxyureido)methyl]phenoxy]butane

HRID 263536
ノート
印刷プレビュー

反応式

HRID 263536 の反応式
[H-].[Na+].[CH2:3]([O:10][NH:11][C:12]([NH2:14])=[O:13])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.Cl[CH2:16][C:17]1[CH:36]=[CH:35][C:20]([O:21][CH2:22][CH2:23][CH2:24][CH2:25][O:26][C:27]2[CH:32]=[CH:31][C:30]([CH2:33]Cl)=[CH:29][CH:28]=2)=[CH:19][CH:18]=1.Cl>CN(C)C=O>[CH2:3]([O:10][N:11]([CH2:16][C:17]1[CH:36]=[CH:35][C:20]([O:21][CH2:22][CH2:23][CH2:24][CH2:25][O:26][C:27]2[CH:32]=[CH:31][C:30]([CH2:33][N:11]([O:10][CH2:3][C:4]3[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=3)[C:12]([NH2:14])=[O:13])=[CH:29][CH:28]=2)=[CH:19][CH:18]=1)[C:12]([NH2:14])=[O:13])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 24758Sodium hydrideHCID 231398BenzyloxyureaHCID 190384131,4-Bis(4-chloromethylphenoxy)butane

生成物 1

HCID 542130111,4-Bis[4-[(1-benzyloxyureido)methyl]phenoxy]butane収率 63.2%

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

反応条件

温度
80 °C

実験手順

60% Sodium hydride (0.41 g) and 1.71 g of benzyloxyurea were added to 20 ml of dimethylformamide and the mixture was stirred at 80° C. for 7.5 hours. 1,4-Bis(4-chloromethylphenoxy)butane (1.74 g) was added to the reaction mixture at room temperature and the mixture was stirred at 95° C. for 0.5 hour. The reaction product was cooled to room temperature, poured into ice water, mixed with 1N hydrochloric acid and then extracted with ethyl acetate. The organic layer was washed with water and saturated sodium chloride aqueous solution in that order and dried over anhydrous magnesium sulfate and then the solvent was evaporated under a reduced pressure. The resulting crude product was washed with ethyl acetate to obtain 1.94 g of 1,4-bis[4-[(1-benzyloxyureido)methyl]phenoxy]butane.

後処理

  1. stirringthe mixture was stirred at 95° C. for 0.5 hour
  2. temperatureThe reaction product was cooled to room temperature
  3. extractionextracted with ethyl acetate
  4. washThe organic layer was washed with water and saturated sodium chloride aqueous solution in that order
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was evaporated under a reduced pressure
  7. washThe resulting crude product was washed with ethyl acetate

出典と根拠

ORDレコード
ord-b6ddbc7cf4a0424f8ca1050d7058a9e0
出典データセット
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05643931

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート