Reacción #674319

Ecuación de reacción

compound

tert-butyl (R)-2-(hydroxymethyl)pyrrolidine-1-carboxylate

phenol

triphenylphosphine

diisopropyl azodicarboxylate

→

tert-butyl (R)-2-(phenoxymethyl)pyrrolidine-1-carboxylate

Disolventes

DCM

toluene

ether

Condiciones de reacción

Tratamiento posterior

1. 1
   Extracciónthe solution was extracted with aqueous 3N NaOH
2. 2
   LavadoThe organic layer was washed with brine
3. 3
   Secadodried over MgSO4
4. 4
   Concentraciónconcentrated in vacuo

Procedimiento

To an ice-cold solution of the compound from Step 1 (2.60 g, 12.9 mmol), phenol (3.64 g, 38.7 mmol), and triphenylphosphine (6.77 g, 25.8 mmol) in DCM (50 mL) was added a solution of diisopropyl azodicarboxylate (5.22 g, 25.8 mmol) in toluene (30 mL). After stirring at room temperature for 60 hours it was diluted with ether and the solution was extracted with aqueous 3N NaOH. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The intermediate tert-butyl (R)-2-(phenoxymethyl)pyrrolidine-1-carboxylate was obtained from the residue by column chromatography (silica gel, cHex/EtOAc 29:1); yield: 1.82 g (51%).

Fuente