Reacción #86878

ord-d224cb5a88ec453f865a2f1872d841c9

Ecuación de reacción

O=C(O)Cc1ccccc1Cl
2-(2-chlorophenyl)acetic acid
CCOC(=O)C(N)=NO
ethyl 2-amino-2-(hydroxyimino)acetate
CCN(C(C)C)C(C)C
N,N diisopropylethylamine
O=C(Cl)C(=O)Cl
oxalyl chloride
CCOC(=O)c1noc(Cc2ccccc2Cl)n1
ethyl 5-(2-chlorobenzyl)-1,2,4-oxadiazole-3-carboxylate
Rendimiento 38.4%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThis compound was prepared
  2. 2
    OtroThe crude material was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane)

Procedimiento

This compound was prepared according to general method 2 with (step I) 2-(2-chlorophenyl)acetic acid (0.646 g; 3.78 mmol) and oxalyl chloride (0.352 mL; 4.16 mmol) in dichloromethane (12 mL) with few drops of DMF and (step II) ethyl 2-amino-2-(hydroxyimino)acetate (0.5 g; 3.78 mmol) and N,N diisopropylethylamine (1.05 mL; 6.06 mmol) in dichloromethane (6 mL) and (step III) pyridine (18 mL). The crude material was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.387 g (38%) of ethyl 5-(2-chlorobenzyl)-1,2,4-oxadiazole-3-carboxylate as a white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09434722B2uspto-grants-2016_09