تفاعل #595346

ord-a7fa4604d7d7428d90a722e1774742b3

معادلة التفاعل

[Al+3].[H-].[H-].[H-].[H-].[Li+]
lithium aluminum hydride
COC(=O)c1ncoc1-c1ccc(Cl)cc1
compound
COC(=O)c1ncoc1-c1ccc(Cl)cc1
Methyl 5-(4-chlorophenyl)-1,3-oxazole-4-carboxylate
O
water
[Na+].[OH-]
sodium hydroxide
OCc1ncoc1-c1ccc(Cl)cc1
[5-(4-Chlorophenyl)-1,3-oxazol-4-yl]methanol

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    درجة الحرارةthe reaction solution is slowly warmed to RT
  3. 3
    workup.STIRRINGWith stirring
  4. 4
    درجة الحرارةthe mixture is then heated
  5. 5
    درجة الحرارةat reflux for 2 h
  6. 6
    درجة الحرارةThe mixture is then cooled again to 0° C.
  7. 7
    workup.STIRRINGthe mixture is stirred at RT for 3 h
  8. 8
    أخرىThe precipitate formed
  9. 9
    ترشيحis filtered off
  10. 10
    أخرىthe filtrate is freed from the solvent on a rotary evaporator
  11. 11
    أخرىThe residue is used without further purification in the subsequent reaction

الإجراء التجريبي

166 mg (4.38 mmol) of lithium aluminum hydride are initially charged in 10 ml of dry THF and cooled to 0° C. A solution of 260 mg (1.09 mmol) of the compound from Example 37A in 10 ml of dry THF is added dropwise. After the addition has ended, the reaction solution is slowly warmed to RT and stirred at this temperature for 1 h. With stirring, the mixture is then heated at reflux for 2 h. The mixture is then cooled again to 0° C., 0.4 ml of water and 0.8 ml of 1 N aqueous sodium hydroxide solution are added carefully and the mixture is stirred at RT for 3 h. The precipitate formed is filtered off, and the filtrate is freed from the solvent 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