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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482713Generated: October 29, 2026

Water → Tert-butyl 3-nitrophenylcarbamate

https://huagongshe.com/reaction/1482713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-NitroanilineHCID 7423—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantEthyl acetate hexaneHCID 21226206—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-nitrophenylcarbamateHCID 1051406582.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 50 mL 3-neck RBF, 3-nitroaniline 5 (5.0 g) in THF (40 mL) and (BOC)2O (7.89 g) was charged and cooled to 0° C. DMAP (6.09 g) was added portion-wise into the reaction mixture and reaction mixture was warmed to room temperature and stirred at room temperature for 5 hr. The reaction was monitored on TLC using hexane:ethyl acetate (5:5) as mobile phase. After completion of the reaction, the reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with 50 mL brine solution, dried over sodium sulfate and concentrated completely under reduced pressure at 40° C. Crude material was purified by using column chromatography. Product was eluted with 4% ethyl acetate in hexane and concentrated to give 7.1 g of tert-butyl(3-nitrophenyl)carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09415049B2
Source datasetuspto-grants-2016_08
ORD IDord-c622b8bff9974e73880f5dbd1e321cd1
Source noteuspto-grants-2016_08