Phosphorus oxychloride → Benzoxazole

HRID 1421226Notes

Reaction equation

HRID 1421226 reaction equation
Br[C:2]1[CH:7]=[C:6](Cl)[CH:5]=[C:4]([N:9](C2C=C(C(C)(C)C)C(O)=C(C(C)(C)C)C=2)[C:10](=O)C)[C:3]=1[OH:28].P(Cl)(Cl)(Cl)=O>C1(C)C=CC=CC=1>[O:28]1[C:3]2[CH:2]=[CH:7][CH:6]=[CH:5][C:4]=2[N:9]=[CH:10]1

Participants

4

Procedure

A solution of 2-bromo-4-chloro-6-(3,5-di-t-butyl-4-hydroxy-phenyl acetyl-amino)-phenol (35.67 g, 76.1 mmol) and phosphorus oxychloride (41.8 ml, 457 mmol) in toluene was heated under reflux for 1 hour. Volatiles were removed in-vacuo and residual amounts of phosphorus oxychloride removed by azeotropic distillation with toluene (2×50 ml). The residue was taken up in acetone (50 ml) and ether (100 ml), and treated with water (100 ml) and saturated aqueous sodium bicarbonate solution (100 ml). The organic solvents were removed in-vacuo and the precipitate collected to give 33.36 g (93.6%) of crude benzoxazole. The crude benzoxazole was dissolved in dichloromethane (100 ml), filtered, and the filtrate diluted with methanol (100 ml). The dichloromethane was removed by distillation and the resulting crystals collected, washed, and dried in-vacuo to give 28.86 g (80.9%) of the title compound (mp 133-6 EC).

Workup

  1. temperatureunder reflux for 1 hour
  2. customVolatiles were removed in-vacuo and residual amounts of phosphorus oxychloride
  3. customremoved by azeotropic distillation with toluene (2×50 ml)
  4. additionether (100 ml), and treated with water (100 ml) and saturated aqueous sodium bicarbonate solution (100 ml)
  5. customThe organic solvents were removed in-vacuo
  6. customthe precipitate collected

Sources & evidence

ORD record
ord-385fbd68edba417ea6704a07b8f8406c
Source dataset
uspto-grants-2000_06
Patent number
US06075016

Reaction notes

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