HRID1377467

反应详情

EQUATION

反应方程式

HRID 1377467 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of 2-(2-amino-5-chlorophenyl)-4-phenyl-1,1,1-trifluoro-3-butyn-2-ol (2.0 g, 6.1 mmol) and 11.0 g (12.0 mmol) of 1,1'-carbonyldiimidazole in 300 mL of dry THF was stirred under argon at 55° C. for 24 hours. The solvent was removed on a rotary evaporator and the residue was partitioned between 200 mL of ether and 400 mL of water. The layers were separated and the aqueous extracted once more with ether. The combined ether extracts were washed with 2×200 mL 10% citric acid and then with brine before drying over MgSO4. Removal of the drying agent and solvent provided 1.5 g (70%) of the crude title compound as an oil. Trituration with ether-hexane afforded 875 mg of (±) 6-chloro-4-phenylethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one as a white solid, partial melt at 137°, clear at 147° C. 1H-NMR (CDCl3): δ6.92 (d, J=8 Hz, 1H), 7.30-7.49 (m, 4H), 7.58-7.65 (m, 3H), 8.99 (s, 1H).

WORKUP

后处理

  1. customThe solvent was removed on a rotary evaporator
  2. customthe residue was partitioned between 200 mL of ether and 400 mL of water
  3. customThe layers were separated
  4. extractionthe aqueous extracted once more with ether
  5. washThe combined ether extracts were washed with 2×200 mL 10% citric acid
  6. dry with materialwith brine before drying over MgSO4
  7. customRemoval of the drying agent and solvent
  8. customprovided 1.5 g (70%) of the crude title compound as an oil