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

5-Bromo-2-(4-methoxybenzyl)-3,3-dimethylisoindolin-1-one → 5-Bromo-3,3-dimethyl-isoindolin-1-one

HRID 605983
ノート
印刷プレビュー

反応式

HRID 605983 の反応式
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[O:11])[N:6](CC1C=CC(OC)=CC=1)[C:5]2([CH3:22])[CH3:21]>C(#N)C.O.C(OCC)(=O)C>[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[O:11])[NH:6][C:5]2([CH3:22])[CH3:21]
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 1

HCID 575899515-Bromo-2-(4-methoxybenzyl)-3,3-dimethylisoindolin-1-one

生成物 1

HCID 575899965-Bromo-3,3-dimethyl-isoindolin-1-one収率 86%

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 6342Acetonitrile溶媒HCID 8857Ethyl Acetate溶媒

実験手順

A solution of 5-bromo-2-(4-methoxybenzyl)-3,3-dimethyl-2,3-dihydroisoindol-1-one (640 mg, 1.78 mmol) and ceric ammonium nitrate (2.91 g, 5.33 mmol) in acetonitrile (11 mL) and water (5 mL) is stirred at 0° C. for 45 min. The solution is diluted with ethyl acetate (100 mL) and washed with brine (40 mL). The organic solvents are dried over MgSO4 and evaporated under reduced pressure. The residue is purified by silica chromatography, eluting with 10% to 50% ethyl acetate in petroleum ether to afford the title compound (367 mg, 1.53 mmol).

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. washwashed with brine (40 mL)
  2. dry with materialThe organic solvents are dried over MgSO4
  3. customevaporated under reduced pressure
  4. customThe residue is purified by silica chromatography
  5. washeluting with 10% to 50% ethyl acetate in petroleum ether

出典と根拠

ORDレコード
ord-b9f7f6bffa3f4d24a70fc5ec56eada44
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07915256B2

反応ノート

読み込み中…