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

Hydroxyamine hydrochloride → HCID 136359213、化合物

HRID 568609
ノート
印刷プレビュー

反応式

HRID 568609 の反応式
[Cl:1][C:2]1[C:16]([Cl:17])=[C:15]([OH:18])[CH:14]=[CH:13][C:3]=1[C:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[F:12])=O.Cl.[NH2:20][OH:21]>N1C=CC=CC=1>[Cl:1][C:2]1[C:16]([Cl:17])=[C:15]([OH:18])[CH:14]=[CH:13][C:3]=1[C:4](=[N:20][OH:21])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[F:12]
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 2

HCID 443297Hydroxyamine hydrochlorideHCID 13015711HCID 13015711、化合物

生成物 1

HCID 136359213HCID 136359213、化合物

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

A solution of 31.8 g of 2,3-dichloro-4-hydroxy-2'-fluoro-benzophenone and 15.3 g of hydroxylamine hydrochloride in 150 ml of pyridine is refluxed for 64 hours. Thereafter, the pyridine is evaporated under vacuum and a 5% aqueous hydrochloric acid solution is added. The acidified solution is extracted with ethyl acetate and the combined extracts are dried before being concentrated to dryness. The resulting solid is recrystallized from an aqueous ethanol solution to yield the product 2,3-dichloro-4-hydroxy-2'-fluorobenzophenone oxime with a melting point of 168° to 175° C.

後処理

  1. customThereafter, the pyridine is evaporated under vacuum
  2. additiona 5% aqueous hydrochloric acid solution is added
  3. extractionThe acidified solution is extracted with ethyl acetate
  4. customthe combined extracts are dried
  5. concentrationbefore being concentrated to dryness
  6. customThe resulting solid is recrystallized from an aqueous ethanol solution

出典と根拠

ORDレコード
ord-f8eebe77ca554918b9e2885fe58a1926
出典データセット
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04728662

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