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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694367Generated: October 30, 2026

Hexamethylenetetramine → 3-(4-Formyl-benzooxazol-2-yl)-benzoic acid methyl ester

https://huagongshe.com/reaction/1694367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethylenetetramineHCID 4101—
ReactantAcetic acid--water (1/1)HCID 21899381—
Reactant3-(4-Bromomethyl-benzooxazol-2-yl)-benzoic acid methyl esterHCID 67279350—
Product3-(4-Formyl-benzooxazol-2-yl)-benzoic acid methyl esterHCID 8606610632%

Reaction Steps

The crude 3-(4-bromomethyl-benzooxazol-2-yl)-benzoic acid methyl ester is treated with HMTA (1.8 mmol) in acetic acid/H2O (3 mL/1.5 mL) in a microwave oven at 130° C. for 20 minutes. The solvent is removed and the mixture is purified by silica gel chromatography (10-20% EtOAc/hexane) to yield 3-(4-formyl-benzooxazol-2-yl)-benzoic acid methyl ester as a white solid. Yield: 32%. 1H NMR (400 MHz, CDCl3) 10.8 (s, 1H), 8.97 (s, 1H), 8.53 (d, J=7.8 Hz, 1H), 8.26 (d, J=7.8 Hz, 1H), 7.94 (dd, J1=7.7 Hz, J2=1 Hz, 1H), 7.86 (d, J=8.1 Hz, 1H), 7.66 (t, J=7.8 Hz, 1H), 7.51 (t, J=7.9 Hz, 1H), 4.0 (s, 3H). LC/MS (ES+): (M+1) 282.1, (M+Na) 304.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158662B2
Source datasetuspto-grants-2012_04
ORD IDord-dc455e9d46a74a8e9c2de4ef374c99ac
Source noteuspto-grants-2012_04