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 → 1-(2,6-Dihydroxyphenyl)-2-methyl-1-propanone oxime

HRID 527533
ノート
印刷プレビュー

反応式

HRID 527533 の反応式
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([OH:8])[C:3]=1[C:9](=O)[CH:10]([CH3:12])[CH3:11].Cl.[NH2:15][OH:16]>N1C=CC=CC=1>[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([OH:8])[C:3]=1[C:9](=[N:15][OH:16])[CH:10]([CH3:12])[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

4

反応物 2

HCID 443297Hydroxyamine hydrochloride2 回HCID 134833211-(2,6-Dihydroxyphenyl)-2-methyl-1-propanone2 回

生成物 1

HCID 1363786541-(2,6-Dihydroxyphenyl)-2-methyl-1-propanone oxime収率 82.1%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

1-(2,6-dihydroxyphenyl)-2-methyl-1-propanone (Intermediate 37, 416 mg) was dissolved in pyridine (2.0 ml) and hydroxylamine hydrochloride (209 mg, 3.0 mmol) was added. The reaction mixture was then stirred at room temperature overnight. After night, additional hydroxylamine hydrochloride (64 mg, 0.92 mmol) was added and the mixture was heated at 100° C. for 3 hours. After removal of the volatiles, the crude was treated with water and extracted with ethyl acetate. The gathered organic layers were dried over sodium sulphate, filtered and evaporated to afford the title compound (370 mg).

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

後処理

  1. waitAfter night
  2. temperaturethe mixture was heated at 100° C. for 3 hours
  3. customAfter removal of the volatiles
  4. additionthe crude was treated with water
  5. extractionextracted with ethyl acetate
  6. dry with materialThe gathered organic layers were dried over sodium sulphate
  7. filtrationfiltered
  8. customevaporated

出典と根拠

ORDレコード
ord-14d6092fb08e4a45b5222e0f7b9b2715
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09346790B2

反応ノート

読み込み中…