Carbon tetrabromide → HCID 69385416, compound

HRID 916839Notes

Reaction equation

HRID 916839 reaction equation
[C:1]([O:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH2:11][CH2:12][CH2:13][CH2:14]O)[CH:6]=1)(=[O:3])[CH3:2].C(Br)(Br)(Br)[Br:17].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C(Cl)Cl>[C:1]([O:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH2:11][CH2:12][CH2:13][CH2:14][Br:17])[CH:6]=1)(=[O:3])[CH3:2]

Participants

5

Procedure

A solution of 3-(4-hydroxybutyl)phenyl acetate (416 mg) in DCM (10 mL) was treated with carbon tetrabromide (1.16 g) and triphenylphosphine (791 mg) and stirred at room temperature for 15 min prior to concentration in vacuo. The residue was purified by chromatography (SPE, DCM-petrol 1:1) to give the title compound. LCMS RT=3.58 min

Workup

  1. concentrationto concentration in vacuo
  2. customThe residue was purified by chromatography (SPE, DCM-petrol 1:1)

Sources & evidence

ORD record
ord-5c0f3dec3e8b4df8aff65ef2f6eb4085
Source dataset
uspto-grants-2007_09
Patent number
US07271197B2

Reaction notes

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