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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955822Generated: October 30, 2026

Triethylamine → 2-[(Tert-butyldimethylsilyl)oxy]-4-nitroaniline

https://huagongshe.com/reaction/1955822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant2-Amino-5-NitrophenolHCID 4984721—
SolventDichloromethaneHCID 6344—
Product2-[(Tert-butyldimethylsilyl)oxy]-4-nitroanilineHCID 1548571084.2%

Reaction Steps

To a magnetically stirred solution of 2-amino-5-nitrophenol (5.62 g, 36.5 mmol) and chloro-t-butyldimethylsilane (5.00 g, 33.2 mmol) in dry dichloromethane (66 mL) was added triethylamine (5.55 mL, 39.8 mmol) at 25° C. The reaction mixture was stirred at ambient temperature for 4 hours and partitioned between diethyl ether (200 mL) and saturated ammonium chloride. The aqueous layer was separated and the ether layer washed (saturated ammonium chloride, 1×; water, 1×; brine, 1×), dried (MgSO4), filtered, and evaporated in vacuo. Crystallization from ethyl acetate/hexanes gave 7.5 g (84%) of O-t-butyldimethylsilyl-2-amino-5-nitrophenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05776984
Source datasetuspto-grants-1998_07
ORD IDord-2576bc4d8518477f964abe22fa1fc887
Source noteuspto-grants-1998_07