تفاعل #595336

ord-9d88209e2aa5464bab63ea959074dc8a

معادلة التفاعل

[Na+].[OH-]
sodium hydroxide
[Al+3].[H-].[H-].[H-].[H-].[Li+]
lithium aluminum hydride
CN1CCOCC1
4-methylmorpholine
CCOC(=O)Cl
ethyl chloroformate
O=C(O)c1nc(-c2ccccc2)oc1C(F)(F)F
2-phenyl-5-(trifluoromethyl)-1,3-oxazole-4-carboxylic acid
OCc1nc(-c2ccccc2)oc1C(F)(F)F
[2-Phenyl-5-(trifluoromethyl)-1,3-oxazol-4-yl]methanol

المذيبات

ظروف التفاعل

درجة الحرارة
-10°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe reaction mixture is stirred overnight
  2. 2
    درجة الحرارةto warm to RT
  3. 3
    درجة الحرارةThe mixture is then once more cooled to 0° C.
  4. 4
    workup.STIRRINGThe mixture is then stirred at RT overnight
  5. 5
    ترشيحAfter filtration
  6. 6
    أخرىthe solvent is removed on a rotary evaporator
  7. 7
    أخرىThe residue is used without further purification in the subsequent reaction

الإجراء التجريبي

500 mg (1.94 mmol) of 2-phenyl-5-(trifluoromethyl)-1,3-oxazole-4-carboxylic acid are dissolved in 40 ml of dry THF and cooled to −10° C. 197 mg (1.94 mmol) of 4-methylmorpholine and 211 mg (1.94 mmol) of ethyl chloroformate are added. The reaction solution is stirred at −10° C. for 1 h. 3.9 ml (3.89 mmol) of a 1 M solution of lithium aluminum hydride in THF are then slowly added dropwise. The reaction mixture is stirred overnight and slowly allowed to warm to RT. The mixture is then once more cooled to 0° C., and 0.6 ml of water and 1.2 ml of 1 N aqueous sodium hydroxide solution are added carefully. The mixture is then stirred at RT overnight. After filtration, the solvent is removed on a rotary evaporator. The residue is used without further purification in the subsequent reaction.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09095582B2uspto-grants-2015_08