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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093749Generated: October 29, 2026

Benzocaine → HCID 58223053, compound

https://huagongshe.com/reaction/2093749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzocaineHCID 2337—
Reactant2,2,2-TrifluoroethanolHCID 6409—
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantCyanuric chlorideHCID 7954—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-HydroxybenzylamineHCID 97472—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 58223053HCID 5822305354.1%

Reaction Steps

To a solution of 2,4,6-trichloro-1,3,5-triazine (10 g) in acetone (210 mL) was added a solution of 2,2,2-trifluoroethanol (5.97 g) and 2,4,6-collidine (7.88 mL) in acetone (210 mL) dropwise over 1 hour. The resulting mixture was stirred at room temperature for 16 hours. All the solvents were removed under vacuum to give a residue which was diluted with NMP (100 mL) and ethyl 4-aminobenzoate (9.85 g), iPr2NEt (28.4 mL) were added. After stirring at room temperature for 6 hours, 4-(aminomethyl)phenol (7.35 g) was added. The resulting mixture was stirred for 16 hours at room temperature. The mixture was diluted with 300 mL of water and extracted with EtOAc (2×500 mL). The organic layers were combined, washed with brine (300 mL), dried over MgSO4 and concentrated. The residue was purified by recrystallization in MeOH to give ethyl 4-(4-(4-hydroxybenzylamino)-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)benzoate (13.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445490B2
Source datasetuspto-grants-2013_05
ORD IDord-dd782571d7024f71b5332e77ce136ed0
Source noteuspto-grants-2013_05