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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188847Generated: November 3, 2026

Difluoroacetic acid → HCID 178498370, compound

https://huagongshe.com/reaction/1188847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDifluoroacetic acidHCID 9788—
ReactantMethyl 2,3-diamino-5-morpholinobenzoateHCID 58279190—
SolventTolueneHCID 1140—
ProductHCID 178498370HCID 178498370—

Reaction Steps

A mixture of methyl 2,3-diamino-5-morpholinobenzoate (40.16 g, 160 mmol) and 2,2-difluoroacetic acid (46.08 g, 480 mmol) in toluene (500 mL) was stirred at reflux temperature for 15 h. Then the mixture was cooled to room temperature and the solvent was removed in vacuum. The residue was purified by silica gel chromatography eluted with petroleum ether:EtOAc=2:1 to afford the desired product. Then, it was dissolved with EtOAc (2 L) and washed with aqueous NaHCO3 (1 L) and brine (1 L). The organic layer was dried over anhydrous Na2SO4 and concentrated to give the desired product (40.9 g, 82%) as a yellow solid. 1H NMR showed this compound is in a form of tautomeric mixture (major tautomer/minor tautomer=5/1) 1H NMR of the major tautomer (300 MHz, DMSO-d6): 6 ppm 3.14 (t, 4H, J=4.8 Hz), 3.78 (t, 4H, J=4.8 Hz), 3.96 (s, 3H), 7.21 (t, 1H, J=52.8 Hz), 7.55 (d, 1H, J=2.4 Hz), 7.65 (d, 1H, J=2.4 Hz), 12.92 (s, 1H); LC-MS: m/e=312 [M+1]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674090B2
Source datasetuspto-grants-2014_03
ORD IDord-fc7736aff8134c19871e282377319cba
Source noteuspto-grants-2014_03