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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065006Generated: October 30, 2026

Methanol → 5-(3-Hydroxymethyl-phenyl)-oxazole-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/2065006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantNitrogenHCID 947—
Reactant5-(3-Carboxy-phenyl)-oxazole-4-carboxylic acid methyl esterHCID 66929300—
SolventTetrahydrofuranHCID 8028—
Product5-(3-Hydroxymethyl-phenyl)-oxazole-4-carboxylic acid methyl esterHCID 66928832—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a suspension of 5-(3-carboxy-phenyl)-oxazole-4-carboxylic acid methyl ester (500 mg, 2.02 mmol) in THF (14.0 mL) at 0° C. was treated dropwise with a BH3 (10.1 mL of a 1M solution in THF, 10.11 mmol). The resulting mixture was stirred at 0° C. for 4 h. MeOH (14 mL) was then added dropwise. After 30 min, the solvent was removed under reduced pressure. EA (20 mL) was added and the organic phase was washed with 1N NaOH (10 mL), water (10 mL) and brine (10 mL). The organic layer was dried over MgSO4, filtered, and the solvent removed under reduced pressure. Purification of the residue by FC (93:7 CH2Cl2-MeOH) gave the title compound as a white solid. TLC: rf (93:7 CH2Cl2-MeOH)=0.32. LC-MS-conditions 02: tR=0.76 min, [M+H]+=234.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288419B2
Source datasetuspto-grants-2012_10
ORD IDord-7ba70068112e40b18161e5928239a4ed
Source noteuspto-grants-2012_10