HRID2179840

反应详情

EQUATION

反应方程式

HRID 2179840 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A glass 3-L four-neck flask was fitted with a mechanical stirrer, a Dimroth condenser, and a dropping funnel. Operating at room temperature, 1 L of pure water was introduced into the reactor followed by the introduction of 69 g (1.93 mol) sodium tetrahydroborate and dissolution. To this was added dropwise 515 g (2.28 mol) 2-hydroxy-3,3,3-trifluoro-2-trifluoromethylpropionic acid methyl ester (MTTHP). Suitable cooling was performed with ice water during this period so as to prevent the liquid temperature from exceeding 50° C. After the dropwise addition of all of the MTTHP, stirring was performed for 1 hour at room temperature and quenching was carried out by the dropwise addition of 300 mL 35% aqueous hydrochloric acid into the reaction solution on an ice bath. The quenched solution was subjected to suction filtration to remove the salts produced during the reaction and the residual salt was washed twice with 500 mL isopropyl ether (IPE). The obtained filtrate was separated and the organic layer was recovered and the aqueous layer was extracted twice with 700 mL IPE. The organic layer and the extracts were combined and dried over magnesium sulfate; suction filtration was performed and the filtrate was recovered; and the IPE was removed by condensation on an evaporator. Simple distillation of the resulting solution under reduced pressure yielded 217 g (isolated yield=48%, purity=98%) 3,3,3-trifluoro-2-trifluoromethylpropane-1,2-diol.

WORKUP

后处理

  1. customOperating at room temperature
  2. temperatureSuitable cooling
  3. customfrom exceeding 50° C
  4. customquenching
  5. additionwas carried out by the dropwise addition of 300 mL 35% aqueous hydrochloric acid into the reaction solution on an ice bath
  6. filtrationThe quenched solution was subjected to suction filtration
  7. customto remove the salts
  8. customproduced during the reaction
  9. washthe residual salt was washed twice with 500 mL isopropyl ether (IPE)
  10. customThe obtained filtrate was separated
  11. customthe organic layer was recovered
  12. extractionthe aqueous layer was extracted twice with 700 mL IPE
  13. dry with materialdried over magnesium sulfate
  14. filtrationsuction filtration
  15. customthe filtrate was recovered
  16. customand the IPE was removed by condensation on an evaporator
  17. distillationSimple distillation of the resulting solution under reduced pressure