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

Potassium Bromide → (2-(Benzyloxy)biphenyl-3-yl)(phenyl)methanone

HRID 45460
ノート
印刷プレビュー

反応式

HRID 45460 の反応式
[CH2:1]([O:8][C:9]1[C:14]([CH:15]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[OH:16])=[CH:13][CH:12]=[CH:11][C:10]=1[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Br-].[K+].Cl[O-].[Na+].C(=O)(O)[O-].[Na+]>ClCCl.O.CC1(C)N([O])C(C)(C)CCC1>[CH2:1]([O:8][C:9]1[C:14]([C:15]([C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)=[O:16])=[CH:13][CH:12]=[CH:11][C:10]=1[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 253877Potassium BromideHCID 516892Sodium BicarbonateHCID 23665760Sodium HypochloriteHCID 58238513(2-(Benzyloxy)biphenyl-3-yl)(phenyl)methanol

生成物 1

HCID 58238523(2-(Benzyloxy)biphenyl-3-yl)(phenyl)methanone収率 88.4%

試薬・触媒・溶媒 3

HCID 2724126
Tempo
触媒
HCID 962Water溶媒2 回
HCID 6344Dichloromethane溶媒2 回

実験手順

A solution of crude 24 (50 mmol) in dichloromethane (200 mL) and a solution of potassium bromide (0.7 g) in water (10 mL) were mixed together and stirred in an ice bath. TEMPO (120 mg) was added and a solution of 37% aqueous sodium hypochlorite (48 mL), sodium bicarbonate (5 g) and water (to 100 mL) was added in portions at such a rate that the temperature did not exceed 5° C. Stirring was continued on the ice bath for 20 min. The reaction mixture was diluted with dichloromethane (200 mL) and washed with water (300 mL), 1N hydrochloric acid (300 mL), water (300 mL) and brine (300 mL). The organic layer was dried over sodium sulfate, filtered and the solvent was removed on a rotary evaporator. The crude product (19 g) was purified by chromatography on silica (350 g) with 2% ethyl acetate in heptane (7 L). Pure 25 (16.1 g, 88%) was isolated.

後処理

  1. customdid not exceed 5° C
  2. stirringStirring
  3. washwashed with water (300 mL), 1N hydrochloric acid (300 mL), water (300 mL) and brine (300 mL)
  4. dry with materialThe organic layer was dried over sodium sulfate
  5. filtrationfiltered
  6. customthe solvent was removed on a rotary evaporator
  7. customThe crude product (19 g) was purified by chromatography on silica (350 g) with 2% ethyl acetate in heptane (7 L)

出典と根拠

ORDレコード
ord-ca5c1650bd1d4738b4ba3bf245bbc7a2
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08541522B2

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