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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938110Generated: October 27, 2026

Hydrochloric Acid → (+)-2-(4-(1-Propanoyloxyethyl)phenyl}-5-decyloxypyrimidine

https://huagongshe.com/reaction/1938110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantPropionyl chlorideHCID 62324—
Reactant2-(4-(1-Hydroxyethyl)phenyl)-5-decyloxypyrimidineHCID 21468280—
SolventWaterHCID 962—
Product(+)-2-(4-(1-Propanoyloxyethyl)phenyl}-5-decyloxypyrimidineHCID 2146827097%

Reaction Steps

Into 20 ml of pyridine were dissolved 1.78 g (5 millimole) of the (+)-2-{4-(1-hydroxyethyl)phenyl}-5-decyloxypyrimidine obtained in the Preparation Example [starting material compound (VI)] 70, and then 0.56 g (6 millimole) of propionic chloride was added thereto, to subject to reaction at 30° to 40° C. for 2 hours. After completion of the reaction, the reaction mixture was poured into 200 ml of water, adjusted to pH 1 to 2 with 4N hydrochloric acid, and then extracted with 200 ml of toluene, followed by separation thereof. The organic phase was washed with water, 5% aqueous sodium hydrogen carbonate solution and water in this order. After drying over anhydrous magnesium sulfate, the residue obtained by distilling the organic solvent off under reduced pressure was purified by silica gel column chromatography (eluent; toluene:ethyl acetate) to obtain 2.00 g (yield: 97%) of (+)-2-{4-(1-Propanoyloxyethyl)phenyl}-5-decyloxypyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05693251
Source datasetuspto-grants-1997_12
ORD IDord-32fce9d0742b45b0a168a623e8ef4054
Source noteuspto-grants-1997_12