Aluminum isopropoxide → 2-Azido-2-(3-bromophenyl)ethan-1-ol

HRID 1825049Notes

Reaction equation

HRID 1825049 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]2[CH2:10][O:9]2)[CH:5]=[CH:6][CH:7]=1.[N:11]([Si](C)(C)C)=[N+:12]=[N-:13].CC(C)[O-].[Al+3].CC(C)[O-].CC(C)[O-].C(C(C(C([O-])=O)O)O)([O-])=O.[K+].[Na+]>C(Cl)Cl>[N:11]([CH:8]([C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([Br:1])[CH:3]=1)[CH2:10][OH:9])=[N+:12]=[N-:13]

Participants

6

Procedure

To a solution of 2-(3-bromo-phenyl)-oxirane (2.5 g, 12.6 mmol) in CH2Cl2 (20 mL) was added azidotrimethylsilane (2.5 mL, 18.84 mmol), followed by aluminium isopropoxide (256 mg, 1.26 mmol). The reaction mixture was stirred at room temperature for 18 h. Sodium potassium tartrate 1M (30 mL) was added, the aqueous layer was extracted with CH2Cl2, and the organic layers were dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated in vacuo, and the crude compound is purified by flash chromatography (10% EtOAc/Hex) to provide 2-azido-2-(3-bromo-phenyl)-ethanol (876 mg, 29%). To a solution of 2-azido-2-(3-bromo-phenyl)-ethanol (876 mg) in THF (10 mL) was added polymer supported triphenylphosphine (3 mmol/g) (2 g, 6 mmol), and the mixture was heated to 60° C. for 30 min. The polymer was then filtered and washed with CH2Cl2. The polymer was suspended in THF (20 mL) and concentrated NH4OH (10 mL) was added, and this mixture was agitated for 24 h. The polymer was filtered and the liquid phase was evaporated in vacuo to afford the title compound (110 mg, 14%).

Workup

  1. extractionthe aqueous layer was extracted with CH2Cl2
  2. dry with materialthe organic layers were dried over anhydrous magnesium sulfate
  3. filtrationfiltered
  4. concentrationThe filtrate was concentrated in vacuo
  5. customthe crude compound is purified by flash chromatography (10% EtOAc/Hex)

Sources & evidence

ORD record
ord-1a34632c1a494f80923ef844923a5cde
Source dataset
uspto-grants-2006_05
Patent number
US07045551B2

Reaction notes

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