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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493310Generated: October 25, 2026

Ethylene carbonate → 2-(1,3-Benzoxazol-4-yloxy)ethanol

https://huagongshe.com/reaction/493310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene carbonateHCID 7303—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Benzoxazol-4-olHCID 13720697—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(1,3-Benzoxazol-4-yloxy)ethanolHCID 22036392—

Reaction Conditions

Temperature90 °C

Reaction Steps

K2CO3 (254 mg, 1.84 mmol) was added to a stirred solution of 4-hydroxybenzoxazole* (248 mg, 1.84 mmol) in DMF (5 mL) at room temperature. The mixture was heated at 90° C. for 15 min and ethylene carbonate (176 mg, 2.00 mmol) was added. The mixture was stirred at 150° C. for 2 h and allowed to attain room temperature. The mixture was diluted with water (2 mL) and MeOH (2 mL), and concentrated. The residue was partitioned between water and CH2Cl2. The aqueous layer was separated and extracted with CH2Cl2 (2×10 mL). The organic phases were pooled and washed with water and brine, and dried over MgSO4. The filtrate was concentrated to give the product as a brown oil that slowly solidified: yield 278 mg (84%), mp 47-49° C. Anal (C9H9NO3) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534794B2
Source datasetuspto-grants-2009_05
ORD IDord-cc74601e8b4f4fbdbb8e56bcc197d43c
Source noteuspto-grants-2009_05