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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184138Generated: November 1, 2026

tert-Butanol → tert-Butyl (5-methoxy-2-nitrophenyl)carbamate

https://huagongshe.com/reaction/1184138

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant5-Methoxy-2-nitrobenzoic acidHCID 339209—
SolventTolueneHCID 1140—
Producttert-Butyl (5-methoxy-2-nitrophenyl)carbamateHCID 10199249—

Reaction Conditions

Temperature95 °C

Reaction Steps

5-Methoxy-2-nitrobenzoic acid (10.30 g) was suspended in toluene (200 ml), triethylamine (9 ml) and diphenylphosphoryl azide (14 ml) were added dropwise at room temperature, and the mixture was stirred at 95° C. for 1.5 hr. Triethylamine (29 ml) and 2-methylpropan-2-ol (15 ml) were added, and the mixture was further stirred at 95° C. for 3 hr. The reaction mixture was concentrated under reduced pressure, and diluted with ethyl acetate. 0.5M Hydrochloric acid (200 ml) was added, and the mixture was filtered through celite. The organic layer of the filtrate was collected, washed with saturated aqueous sodium hydrogen carbonate, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, and a fraction eluted with ethyl acetate-hexane (5:95-1:1) was concentrated under reduced pressure to give the object product (13.28 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664380B2
Source datasetuspto-grants-2014_03
ORD IDord-43b8e86bcb8144e8be3485f66b1d74b3
Source noteuspto-grants-2014_03