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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294277Generated: November 4, 2026

Hydrochloric Acid → HCID 68885486, compound

https://huagongshe.com/reaction/1294277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl (2-hydroxyphenyl)acetateHCID 89719—
ReactantHCID 17861373HCID 17861373—
SolventDimethylformamideHCID 6228—
ProductHCID 68885486HCID 6888548649.2%

Reaction Steps

A mixture of 4-(4-chloromethyl-3-methoxyphenoxymethyl)-2-phenyl-5-methyloxazole (2.08 g), methyl 2-(2-hydroxyphenyl)acetate (1.00 g), anhydrous potassium carbonate (1.65 g) and N,N-dimethylformamide (15 mL) was stirred overnight at room temperature. The reaction mixture was poured into dilute hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. To a mixture of the obtained residue, tetrahydrofuran (10 mL) and methanol (10 mL) was added a 1N aqueous sodium hydroxide solution (10 mL) and the mixture was stirred at room temperature for 2 hrs. The reaction mixture was concentrated, and dilute hydrochloric acid was added to the residue. The precipitated solid was collected by filtration and dried with air to give crystals (1.36 g, 49%) of 2-[2-[3-methoxy-4-[(2-phenyl-5-methyl-4-oxazolyl)methoxy]benzyloxy]phenyl]acetic acid. Recrystallization from acetone-hexane gave colorless needle crystals. melting point: 165-166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238716B2
Source datasetuspto-grants-2007_07
ORD IDord-ed4bd2de657b4fd380b627b910bc3a0c
Source noteuspto-grants-2007_07