Diethyl Ether → 5-(Chloromethyl)-2-phenyl-1,3-oxazole

A solution of chloracetyl chloride (freshly distilled, 1.59 ml, 20 mmol) in ether (10 ml) was added dropwise to a cooled (0° C.) solution of diazomethane in ether (40 mmol, ex 10.8 g Diazald) and stirred until nitrogen had ceased (ca. 10-15 mins). The solvent was blown off using nitrogen and the residual oil containing the diazoketone used without further purification. The 1-chloro-3-diazo propanone was taken up in dichloromethane (50 ml) and added dropwise to a solution of boron trifluoride etherate (4.9 ml, 40 mmol) and benzonitrile (10.2 ml, 100 mmol) in dichloromethane (150 ml) and stirred until nitrogen evolution had ceased. The mixture was then poured onto 20% aqueous sodium hydroxide solution (300 ml), the organic layer separated, washed with brine and dried (MgSO4). Solvent removal then distillation at reduced pressure gave an oil which was further purified by column chromatography (CH2Cl2 as eluant, 20 g silica) to give the title compound (870 mgs, 4.50 mmol, 22%); Vmax (film), 3060, 2960, 1665, 1610, 1550, 1545, 1480, 1450, 1355, 1280, 1125, 1040, 1020, 990, 900, 875, 840, 780, 700 cm-1 ; δH (CDCl3) 4.60 (2H, s, CH2 --Cl), 7.10 (1H, s, CH-4), 7.40 (3H, m, Ph), 7.90 (2H, m, Ph).

1. distillationA solution of chloracetyl chloride (freshly distilled
2. addition1.59 ml, 20 mmol) in ether (10 ml) was added dropwise to
3. custom(ca. 10-15 mins)
4. customused without further purification
5. stirringstirred until nitrogen evolution
6. customthe organic layer separated
7. washwashed with brine
8. dry with materialdried (MgSO4)
9. customSolvent removal
10. distillationdistillation at reduced pressure
11. customgave an oil which
12. customwas further purified by column chromatography (CH2Cl2 as eluant, 20 g silica)

ORD record

ord-9081251301f044c28f806ff6ad4bf166

Source dataset

uspto-grants-1989_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04812470