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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769779Generated: October 30, 2026

Water → HCID 10785546, compound

https://huagongshe.com/reaction/1769779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThionyl ChlorideHCID 24386—
Reactant3,3,3-Trifluoro-2-hydroxy-2-methylpropanoic acidHCID 2775125—
Reactant4'-Amino-2,3-difluorobenzophenoneHCID 10823516—
SolventDimethylacetamideHCID 31374—
ProductHCID 10785546HCID 1078554670.4%

Reaction Steps

To a stirred, cooled (-20° C.) solution of 3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acid (1.02 g, 6.4 mmol) in N,N-dimethylacetamide (10 mL) was added thionyl chloride (0.77 g, 6.4 mmol) and the mixture stirred at -10° to -15° C. for 1 hour. 4'-Amino-2,3-difluorobenzophenone (1.00 g, 4.3 mmol) was added in one portion and the reaction mixture stirred at room temperature overnight. The mixture was poured into water and the aqueous solution extracted with methylene chloride (2×50 mL). The combined organics were washed with water and 3N HCl (1×50 mL), dried (MgSO4) and concentrated in vacuo to yield a tan solid. The solid was purified by flash column chromatography (5% v/v ethyl acetate/methylene chloride). Recrystallization of the resulting solid from methylene chloride/hexane yielded the title propanamide as a white solid (1.13 g, 70%); mp 154°-155° C. 1H-NMR (250 MHz, d 6-DMSO): 1.60 (s, 3H, CH3) 7.36-7.40 (m, 2H, aromatic) 7.57 (s, 1H, OH) 7.65-7.72 (m, 1H, aromatic) 7.89 (d, 2H, J=8.6 Hz, aromatic) 7.98 (d, 2H, J=8.6 Hz, aromatic) 10.40 (s, 1H, NH). MS (CI, CH4): 374 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05382598
Source datasetuspto-grants-1995_01
ORD IDord-d655418e3dfd413da3ed8d7dcdf6b287
Source noteuspto-grants-1995_01