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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711546Generated: October 31, 2026

Pyridine → HCID 23093508, compound

https://huagongshe.com/reaction/1711546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl AcetateHCID 8857—
Reactant4-(Trifluoromethoxy)benzoyl ChlorideHCID 142110—
ProductHCID 23093508HCID 23093508—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of tert-butyl 2-hydroxyethyl (methyl)carbamate (1.30 g) obtained in Reference Example 1 and ethyl acetate (10 mL) were added 4-trifluoromethoxybenzoyl chloride (1.83 g) and pyridine (0.72 mL). The mixture was stirred at 60° C. for 25 hrs. Ethyl acetate (60 mL) was added to the reaction mixture, and the mixture was washed with water (30 mL), a saturated aqueous sodium hydrogen carbonate solution (20 mL) and water (20 mL), and dried over anhydrous magnesium sulfate. After concentration under reduced pressure, a 4N hydrogen chloride—ethyl acetate solution (10 mL) was added to the residue. After stirring at room temperature for 14.5 hrs., the mixture was concentrated under reduced pressure. The residue was washed twice with ethyl acetate (15 mL), and dried under reduced pressure at 60° C. to give the title compound (1.83 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790755B2
Source datasetuspto-grants-2010_09
ORD IDord-a36c531aa1f0461cb1ccc5dbb1676f65
Source noteuspto-grants-2010_09