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

HRID 1914846
ノート
印刷プレビュー

反応式

HRID 1914846 の反応式
[Br:1][C:2]1[CH:9]=[CH:8][C:5](C=C)=[CH:4][CH:3]=1.[NH+]1([O-])[CH2:15][CH2:14][O:13]CC1.S([O-])([O-])(=[O:19])=S.[Na+].[Na+]>CC(C)=O.O.O=[Os](=O)(=O)=O>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:14]([OH:13])[CH2:15][OH:19])=[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

7

反応物 3

HCID 162634-BromostyreneHCID 24477Sodium ThiosulfateHCID 15900019Morpholine oxide

生成物 1

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

試薬・触媒・溶媒 3

HCID 30318Osmium Tetroxide触媒2 回HCID 180Acetone溶媒
HCID 962
Water
溶媒
2 回

実験手順

To 4-bromostyrene (Compound [LXI], 366 mg, 2 mmol, 1 eq.) in acetone (10 mL) was added morpholine N-oxide (953 mg of a 50% solution in H2O, 4.0 mmol, 2.0 eq.) and then OsO4 (1.3 g for a 4% OsO4 in H2O, 0.2 mmol, 0.1 eq). The mixture was allowed to stir at room temperature for 1 hour. The reaction mixture was then added to an aqueous solution of sodium thiosulfate and then extracted three times with EtOAc. The combined organics were dried over Na2SO4, concentrated, and subjected to silica gel chromatography using EtOAc-heptane as the eluant to provide Compound [LXII]: 1H NMR (400 MHz, METHANOL-d4) δ ppm 3.54-3.66 (m, 2H) 4.66 (dd, J=6.76, 5.10 Hz, 1H) 7.24-7.35 (m, 2H) 7.41-7.53 (m, 2H).

後処理

  1. extractionextracted three times with EtOAc
  2. dry with materialThe combined organics were dried over Na2SO4
  3. concentrationconcentrated
  4. customto provide Compound [LXII]

出典と根拠

ORDレコード
ord-540b65ed130f48c8aba26cb93484e3f3
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08614221B2

反応ノート

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