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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165541Generated: October 28, 2026

Triethylamine → 2,6-Dichloro-N-trimethylsilylaniline

https://huagongshe.com/reaction/1165541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,6-DichloroanilineHCID 11846—
ReactantBromotrimethylsilaneHCID 76113—
SolventBenzeneHCID 241—
Product2,6-Dichloro-N-trimethylsilylanilineHCID 1436267975.1%

Reaction Steps

A solution of 60 ml of benzene, 5.0 g (30.9 mmole) of 2,6-dichloroaniline, 10.6 ml (76.0 mmole) of triethylamine, and 8.08 ml (61.1 mmole) of trimethylsilyl bromide was heated at reflux for 54 hours, cooled, filtered, and the solvent was removed from the filtrate in vacuo. The residue was evacuated at 1 mm to remove any excess trimethylsilyl bromide. The residual mixture was filtered into a round-bottomed flask and distilled using a short Vigreaux column to provide 5.43 g (23.2 mmole, 75.0 percent yield) of the N-trimethylsilyl-2,6-dichloroaniline as a 97 percent pure amber oil, bp 74° C.-75° C. at 0.4 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04910306
Source datasetuspto-grants-1990_03
ORD IDord-ce9fdf01c75b4c6fb2f6d34b35bd44d1
Source noteuspto-grants-1990_03