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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22714Generated: October 25, 2026

Trimethyl orthoacetate → 5-Methoxy-2-methylbenzoxazole

https://huagongshe.com/reaction/22714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoacetateHCID 15050—
Reactant2-Amino-4-methoxyphenolHCID 1419108—
Product5-Methoxy-2-methylbenzoxazoleHCID 79759—

Reaction Steps

A solution of 2-amino-4-methoxyphenol 17 (8 g, 57.4 mmol) in trimethyl orthoacetate 18 (50 mL) was heated to reflux and allowed to stir for 24 h. The reaction was allowed to cool and the excess 18 was evaporated (in vacuo). The residue was dissolved in ethyl acetate and washed with water. The organic layer was dried over MgSO4 and treated with activated carbon Norit A. The resulting solution was filtered through Celite 521 and evaporated to yield an oil. The oil was chromatographed on silica gel (20% ethyl acetate/hexanes) to yield compound 19 as a light yellow solid. Synthesis of 2-methyl-5-oxiran-2-ylmethoxybenzoxazole (67):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849632B2
Source datasetuspto-grants-2005_02
ORD IDord-c0bca52f05014ddbbde713850ce9dfda
Source noteuspto-grants-2005_02