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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539227Generated: October 26, 2026

Difluoroacetic acid → HCID 178498370, compound

https://huagongshe.com/reaction/539227

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): δ 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 numberUS08865912B2
Source datasetuspto-grants-2014_10
ORD IDord-7fae73658a1c4c29bef88d3f99c1d3f8
Source noteuspto-grants-2014_10