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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37327Generated: October 29, 2026

Triethylamine → 1-(4-Tert-butyldimethylsiloxy-3,5-dichlorophenyl)-3-(2,6-difluorobenzoyl)urea

https://huagongshe.com/reaction/37327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 14275603HCID 14275603—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-(4-Tert-butyldimethylsiloxy-3,5-dichlorophenyl)-3-(2,6-difluorobenzoyl)ureaHCID 1907290265.8%

Reaction Steps

Into a homogeneous solution of 1-(3,5-dichloro-4-hydroxyphenyl)-3-(2,6-difluorobenzoyl)urea (3.13 grams, 8.66 mmol) in dimethylformamide (25 milliliters) was added triethylamine (1.75 grams, 17.3 mmol), and the resulting mixture was stirred for 5 minutes. Tertiary-butyldimethylsilyl chloride (3.92 grams, 26.0 mmol) was then added, and a thick precipitate formed immediately. This heterogeneous mixture was then diluted with ethyl acetate (200 milliliters), washed with saturated sodium bicarbonate (twice with 150 milliliters) and then washed with a brine solution (150 milliliters). The organic layer was dried over sodium sulfate, filtered, and concentrated under reduced pressure to give a brown solid. The solid was washed with cold ether and vacuum dried to afford 1-(4-tert-butyldimethylsiloxy-3,5-dichlorophenyl)-3-(2,6-difluorobenzoyl)urea (2.71 grams, 5.70 mmol) having a melting point of 184° C.-186° C. Elemental analysis of the product indicated the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420163
Source datasetuspto-grants-1995_05
ORD IDord-8346b002bf8a41d6bf780cd1df85aa57
Source noteuspto-grants-1995_05