Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760864Generated: November 1, 2026

tert-Butanol → Methyl 2-((tert-butoxycarbonyl)amino)-3-nitrobenzoate

https://huagongshe.com/reaction/1760864

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2-(Methoxycarbonyl)-6-nitrobenzoic acidHCID 4399477—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-((tert-butoxycarbonyl)amino)-3-nitrobenzoateHCID 996596870%

Reaction Steps

To a solution of methyl 2-carboxy-3-nitrobenzoate (7.23 g) in DMF (50 ml) was added diphenylphosphoryl azide (11.3 g) at room temperature and then triethylamine (6.7 ml) was added dropwise to the stirred reaction mixture. After stirring at room temperature for 3 Hours, tert-butanol (54 ml) was added to the stirred reaction mixture. After stirring at room temperature for 30 min., the reaction mixture was gradually warmed, then heated under reflux for 1 hour and evaporated to dryness. The resultant residue was dissolved in ethyl acetate, washed with dilute hydrochloric acid, aqueous sodium bicarbonate, and water, and then dried. After evaporation of the solvent, methanol was added to the resultant residue and the mixture was cooled to give colorless crystals (6.7 g, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06844443B2
Source datasetuspto-grants-2005_01
ORD IDord-433f9552eb5c4f14a687ab701c8c237e
Source noteuspto-grants-2005_01