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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042714Generated: November 2, 2026

Triethylamine → Ammonium Hydroxide

https://huagongshe.com/reaction/1042714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromoacetyl bromideHCID 61147—
Reactant2-Tert-butyl-5-nitroanilineHCID 826103—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductAmmonium HydroxideHCID 14923—
Product2-bromo-N-(2-tert-butyl-5-nitrophenyl)acetamideHCID 21961385—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-tert-Butyl-5-nitrobenzenamine (70 g, 359 mmol) and a catalytic amount of DMAP were dissolved into THF (1.5 L) under N2. Triethylamine (109 g, 1077 mmol) was added and the solution was cooled to 0° C. Bromoacetyl bromide (207 g, 1023 mmol) was then added and the reaction was stirred at room temperature for 16 hours. The reaction was then partially concentrated under reduced pressure, treated with water, and extracted three times with EtOAc. The EtOAc extracts were washed with brine, combined, dried over Na2SO4 and concentrated to a black oil. The oil was purified using silica chromatography, 95:5:0.5 CH2Cl2:MeOH:NH4OH, giving 2-bromo-N-(2-tert-butyl-5-nitrophenyl)acetamide as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557996B2
Source datasetuspto-grants-2013_10
ORD IDord-b5b30d1eeae0461cbee1c135b7a329d5
Source noteuspto-grants-2013_10