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

HRID 1914846
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HRID 1914846 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 162634-BromostyreneHCID 24477Sodium ThiosulfateHCID 15900019Morpholine oxide

생성물 1

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

시약·촉매·용매 3

HCID 30318Osmium Tetroxide촉매2회HCID 180Acetone용매
HCID 962
Water
용매
2회

실험 절차

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).

후처리

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

출처 및 근거

ORD 기록
ord-540b65ed130f48c8aba26cb93484e3f3
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08614221B2

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