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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860937Generated: October 31, 2026

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

https://huagongshe.com/reaction/860937

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 absolution 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 numberUS07153972B2
Source datasetuspto-grants-2006_12
ORD IDord-6e453d49bfe545c799086343b7d2fc57
Source noteuspto-grants-2006_12