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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
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Water → 3-(2,5-Dichlorophenoxy)-1,1-dimethyl urea

HRID 1195603
ノート
印刷プレビュー

反応式

HRID 1195603 の反応式
[Cl:1][C:2]1[CH:9]=[CH:8][C:7]([Cl:10])=[CH:6][C:3]=1[O:4][NH2:5].[CH3:11][N:12]([CH3:16])[C:13](Cl)=[O:14].O>N1C=CC=CC=1>[Cl:1][C:2]1[CH:9]=[CH:8][C:7]([Cl:10])=[CH:6][C:3]=1[O:4][NH:5][C:13](=[O:14])[N:12]([CH3:16])[CH3:11]
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 6598Dimethylcarbamoyl ChlorideHCID 135748982,5-Dichlorophenoxyamine

生成物 1

HCID 137463693-(2,5-Dichlorophenoxy)-1,1-dimethyl urea収率 61.9%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

5.00 g (28.1 mmoles) of 2,5-dichlorophenoxyamine was dissolved in 6.8 ml of pyridine, and then 3.02 g (28.1 mmoles) of dimethylcarbamoyl chloride was added. The mixture was stirred at a temperature of from 25° to 30° C. for 12 hours. After an addition of 200 ml of water, the reaction mixture was extracted with ethyl acetate. The extract was washed with a saturated sodium chloride aqueous solution, and dried over anhydrous magnesium sulfate. Ethyl acetate was distilled off under reduced pressure, and precipitated crystals were washed with hexane, whereby 4.33 g of the desired product was obtained as light yellow crystals (yield: 62%).

後処理

  1. extractionthe reaction mixture was extracted with ethyl acetate
  2. washThe extract was washed with a saturated sodium chloride aqueous solution
  3. dry with materialdried over anhydrous magnesium sulfate
  4. distillationEthyl acetate was distilled off under reduced pressure
  5. customprecipitated crystals
  6. washwere washed with hexane

出典と根拠

ORDレコード
ord-222da86cfe2049e598b5543dd9a81609
出典データセット
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05112385

反応ノート

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