Reacción #725913

ord-9ce7e10b3e064126910f5122238cbfc1

Ecuación de reacción

C(=NC1CCCCC1)=NC1CCCCC1
1,3-dicyclohexyl carbodiimide
O=C(O)COc1ccc([N+](=O)[O-])cc1
(4-nitrophenoxy)acetic acid
O=C(O)COc1ccc([N+](=O)[O-])cc1
(4-Nitro phenoxy) acetic acid
O=C(COc1ccc([N+](=O)[O-])cc1)OCCO
(4-nitro-phenoxy)acetic acid-2-hydroxyethyl ester
O=C(COc1ccc([N+](=O)[O-])cc1)OCCO
(4-Nitro-phenoxy)-acetic acid-2-hydroxy-ethyl ester
O=C(COc1ccc([N+](=O)[O-])cc1)OCCOC(=O)COc1ccc([N+](=O)[O-])cc1
42
Rendimiento 54.0%
O=C(COc1ccc([N+](=O)[O-])cc1)OCCOC(=O)COc1ccc([N+](=O)[O-])cc1
(4-Nitro-phenoxy)-acetic acid-2-[2-(4-nitro-phenoxy)-acetoxy]-ethyl ester
Rendimiento 54.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe solids were filtered off
  2. 2
    workup.DISTILLATIONdichloromethane distilled off
  3. 3
    Otroto get crude 42
  4. 4
    OtroThe crude 42 was purified by column chromatography on silica gel

Procedimiento

To a mixture of (4-nitrophenoxy)acetic acid 40 (80 g, 406 mmol) and (4-nitro-phenoxy)acetic acid-2-hydroxyethyl ester 41 (80 g, 332 mmol) in anhydrous dichloromethane (2 L) under nitrogen atm. was added a solution of 1,3-dicyclohexyl carbodiimide (128 g, 620 mmol) in anhydrous dichloromethane (750 ml) drop wise. The reaction mixture was stirred at room temperature for 8 hours. The solids were filtered off and dichloromethane distilled off to get crude 42. The crude 42 was purified by column chromatography on silica gel using hexane:ethyl acetate (95:5) to get pure 42 (75 g, 54%) as a white powder. M.p: 138-139° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07691364B2uspto-grants-2010_04