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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358184Generated: October 30, 2026

2-Chlorobenzoxazole → HCID 13090853, compound

https://huagongshe.com/reaction/358184

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
ReactantPotassium HydroxideHCID 14797—
ReactantN-(2,2,2-trifluoroethyl)-N-methyl-hydroxyacetic acid amideHCID 13090851—
SolventAcetonitrileHCID 6342—
ProductHCID 13090853HCID 1309085352%

Reaction Conditions

Temperature20 °C

Reaction Steps

17.1 g (0.1 mol) of N-(2,2,2-trifluoroethyl)-N-methyl-hydroxyacetic acid amide and 7 g of potassium hydroxide powder were initially introduced into 100 ml of acetonitrile at 20° C., and 15.3 g (0.1 mol) of 2-chlorobenzoxazole were added at a temperature between 20° and 40° C. The reaction mixture was stirred at 40° C. for one hour and at 20° C. for a further 15 hours and was concentrated and the concentrate was shaken with toluene and water. The organic phase was washed with dilute sodium hydroxide solution, washed until neutral, dried and filtered. The solvent was carefully distilled off from the filtrate under reduced pressure. 15 g (52% of theory) of N-(2,2,2-trifluoroethyl)-N-methyl-benzoxazol-2-yl-oxy-acetic acid amide of melting point 92° C. were obtained as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04465504
Source datasetuspto-grants-1984_08
ORD IDord-1a97c3c698a64f23bf2f33a17833901d
Source noteuspto-grants-1984_08