Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089129Generated: October 25, 2026

Acetic Acid → (5-Trifluoromethyl-benzo[d]isoxazol-3-ylamino)-acetic acid

https://huagongshe.com/reaction/2089129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantGlyoxylic acid, monohydrateHCID 15620607—
Reactant5-(Trifluoromethyl)-1,2-benzoxazol-3-amineHCID 43811099—
SolventMethanolHCID 887—
Product(5-Trifluoromethyl-benzo[d]isoxazol-3-ylamino)-acetic acidHCID 58548759—

Reaction Conditions

Temperature80 °C

Reaction Steps

5-Trifluoromethyl-benzo[d]isoxazol-3-ylamine (2.5 g, 12.4 mmol) and glyoxylic acid monohydrate (Aldrich, 1.14 g, 12.4 mmol) in MeOH (10 mL) were treated with a few drop of AcOH and heated at 80° C. for 30 min. The reaction was then cooled to room temperature and NaBCNH3 (Aldrich, 1.17 g, 18.6 mmol) was added in one portion and the resulting solution was stirred at room temperature for another 2 hours. The solvent was removed and the residue was partitioned between ether and 1 N NaOH. The aqueous layer was then acidified with 1 N HCl to pH=3 and then extracted three times with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated to give the title compound as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436023B2
Source datasetuspto-grants-2013_05
ORD IDord-7899549d784d48daa438b804fc2466ec
Source noteuspto-grants-2013_05