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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773396Generated: November 1, 2026

tert-Butanol → 2-Nitro-terephthalic acid 1-tert-butyl ester 4-methyl ester

https://huagongshe.com/reaction/1773396

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant4-(Methoxycarbonyl)-2-nitrobenzoic acidHCID 21906474—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-Nitro-terephthalic acid 1-tert-butyl ester 4-methyl esterHCID 67512782—

Reaction Steps

Commercially available 2-nitro-terephthalic acid 4-methyl ester (4.84 g, 21.49 mmol) in DCM (54 mL) was treated with tert-butanol (4.05 mL, 42.99 mmol), di-tert-butyl dicarbonate (12.19 g, 55.87 g) and DMAP (0.79 g, 6.45 mmol). After 4 days at room temperature, the reaction was diluted with DCM (100 mL), washed with 1N HCl (100 mL), aqueous NaHCO3 and finally with water. After drying over sodium sulphate and evaporation of the volatiles, the title compound was obtained as a brownish oil in more than quantitative yield (6.51 g). The crude was employed in the following step with no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255087B2
Source datasetuspto-grants-2016_02
ORD IDord-1852d564dc654105a9f5f93407a8e857
Source noteuspto-grants-2016_02