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

Nitric Acid → Propane, 1,2-dichloro-2-fluoro-3-nitro-

HRID 893406
ノート
印刷プレビュー

反応式

HRID 893406 の反応式
[N+:1]([O-:4])(O)=[O:2].[Cl:5][C:6]([CH2:8][Cl:9])=[CH2:7].[FH:10]>>[Cl:5][C:6]([F:10])([CH2:8][Cl:9])[CH2:7][N+:1]([O-:4])=[O:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 944Nitric AcidHCID 65652,3-DichloropropeneHCID 14917Hydrofluoric Acid

生成物 1

HCID 10954045Propane, 1,2-dichloro-2-fluoro-3-nitro-

実験手順

To a mixture of 86 ml of anhydrous, 100% strength nitric acid and 300 ml of anhydrous hydrofluoric acid were added dropwise at -10° C. in the course of 3 hours 111 g (1 mol) of 2,3-dichloropropene. The reaction was slightly exothermic. After the dropwise addition had ceased, stirring was continued for a further 1 hour at -10° C. Then the mixture was poured on to ice and extracted using dichloromethane. The organic phase was washed with sodium hydrogencarbonate solution, dried over sodium sulphate and concentrated using a rotary evaporator. The crude product was distilled under an oil pump vacuum. This gave 115.8 g (=63% of theory) of product having a boiling point of 48° to 50° C. at 0.07 mbar and a Refractive Index nD20 of 1.4578 (at 24° C.). The product was 95.7% pure.

後処理

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
  1. additionAfter the dropwise addition
  2. additionThen the mixture was poured on to ice
  3. extractionextracted
  4. washThe organic phase was washed with sodium hydrogencarbonate solution
  5. dry with materialdried over sodium sulphate
  6. concentrationconcentrated
  7. customa rotary evaporator
  8. distillationThe crude product was distilled under an oil pump vacuum
  9. customof 1.4578 (at 24° C.)

出典と根拠

ORDレコード
ord-afec642ef1af4c7c96b1e22144e82fe1
出典データセット
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05124476

反応ノート

読み込み中…