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4-Bromostyrene → 1-(4-bromophenyl)ethane-1,2-diol

HRID 2275732
ノート
印刷プレビュー

反応式

HRID 2275732 の反応式
[Br:1][C:2]1[CH:9]=[CH:8][C:5](C=C)=[CH:4][CH:3]=1.C[N+]1([O-])[CH2:16][CH2:15][O:14]CC1.CC(C)=[O:20].O>CCOC(C)=O.[Os](=O)(=O)(=O)=O>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:15]([OH:14])[CH2:16][OH:20])=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 162634-BromostyreneHCID 82029Methyl morpholine oxideHCID 18366337Propan-2-one--water (1/1)

生成物 1

HCID 111486511-(4-bromophenyl)ethane-1,2-diol収率 28%

試薬・触媒・溶媒 2

HCID 30318Osmium Tetroxide触媒HCID 8857Ethyl Acetate溶媒
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

実験手順

4-Bromostyrene (1.00 g, 5.46 mmol) was dissolved in 25 mls of 2:1 water acetone. To this was added 4-methylmorpholine N-oxide (0.704 g, 6.01 mmole) and osmium tetroxide (0.167 g, 0.061 mmole, 2.5% in t-BuOH). This mixture was stirred at room temperature for 16 hours, then diluted with EtOAc, washed once with 1N aq. HCl, once with saturated sodium bicarbonate solution, dried over sodium sulfate and concentrated under reduced pressure. The resulting crude product was purified by Flash 40 Biotage (40M cartridge, 100% EtOAc as the eluant) to give 335 mgs (28%) of 1-(4-bromophenyl)ethane-1,2-diol as a white solid.

後処理

  1. washwashed once with 1N aq. HCl, once with saturated sodium bicarbonate solution
  2. dry with materialdried over sodium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customThe resulting crude product was purified by Flash 40 Biotage (40M cartridge, 100% EtOAc as the eluant)

出典と根拠

ORDレコード
ord-af1a65da36c3433aaaf9982cd6aa7c25
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09126940B2

反応ノート

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