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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082163Generated: November 3, 2026

Triethylamine → HCID 22915149, compound

https://huagongshe.com/reaction/1082163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 22915050HCID 22915050—
SolventAcetonitrileHCID 6342—
ProductHCID 22915149HCID 2291514969.6%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 12.0 g of 2-bromo-5-hydroxy -3-methoxy-6-methyl-benzoic acid in 700 ml of acetonitrile were added at -5° C. 27.7 g of tert-butyldimethylchlorosilane and 18.5 g of triethylamine. The mixture was stirred for 30 min at -5° C. and for 16 h at 20° C. The solvent was evaporated in vacuo and the solid residue was washed with water and dried in vacuo. A solution of this material in 200 ml of ethanol was heated for 8 h to 80° C. The solvent was evaporated in vacuo and the residue was recrystallized from pentane to yield 12.0 g of 2-bromo-5-(tert-butyl-dimethylsilanyloxy)-3-methoxy-6-methyl-benzoic acid as white crystals, m.p. 120°-125° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05589473
Source datasetuspto-grants-1996_12
ORD IDord-da4446dbffd944f0a039c90c079754bf
Source noteuspto-grants-1996_12