Reacción #217454

ord-2a05641a385e4dafafa03acb0082da18

Ecuación de reacción

CN(C)C=O
dimethylformamide
CCC1(COCCCCCCBr)COC1
3-[(6-bromohexyloxy)methyl]-3-ethyloxetane
O=C(O)c1ccc(O)cc1
4-hydroxybenzoic acid
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCC1(COCCCCCCOc2ccc(C(=O)O)cc2)COC1
4-[6-(3-ethyloxetane-3-ylmethoxy)hexyloxy]benzoic acid
Rendimiento 66.4%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónit was extracted with toluene 4 L
  2. 2
    LavadoThe organic layer was washed with water
  3. 3
    workup.DISTILLATIONthe solvent was distilled off
  4. 4
    workup.ADDITIONSodium hydroxide 200 g, water 1 L and ethanol 2.5 L were added to the resulting residue
  5. 5
    Temperaturarefluxed for 4 hours
  6. 6
    workup.DISTILLATIONEthanol (1 L) was distilled off at atmospheric pressure
  7. 7
    Otroto obtain a slurry
  8. 8
    FiltraciónThe slurry was filtered
  9. 9
    Otrodried

Procedimiento

A dimethylformamide (3 L) solution of 3-[(6-bromohexyloxy)methyl]-3-ethyloxetane 500 g, 4-hydroxybenzoic acid 297 g and potassium carbonate 490 g was stirred at 90° C. for 8 hours. Water 4 L was added to the reaction mixture, and then it was extracted with toluene 4 L. The organic layer was washed with water, and the solvent was distilled off. Sodium hydroxide 200 g, water 1 L and ethanol 2.5 L were added to the resulting residue and refluxed for 4 hours. Ethanol (1 L) was distilled off at atmospheric pressure, and then the solution was acidified by hydrochloric acid to obtain a slurry. The slurry was filtered and dried to thereby obtain 400 g of 4-[6-(3-ethyloxetane-3-ylmethoxy)hexyloxy]benzoic acid. Melting point: 58.5° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07381350B2uspto-grants-2008_06