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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768449Generated: October 31, 2026

Trimethylamine → [(15-Bromopentadecyl)oxy](tert-butyl)dimethylsilane

https://huagongshe.com/reaction/1768449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylamineHCID 1146—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant15-Bromopentadecan-1-olHCID 543850—
SolventDichloromethaneHCID 6344—
Product[(15-Bromopentadecyl)oxy](tert-butyl)dimethylsilaneHCID 2361517494.4%

Reaction Steps

15-Bromo-pentadecan-1-ol (2.3 g, 7.49 mmol) dissolved in methylene chloride (23 mL) was mixed with trimethylamine (2.1 mL, 14.98 mmol), t-butyldimethylsilyl chloride (2.03 g, 13.48 mmol), and dimethylaminopyridine (457.6 mg, 3.74 mmol). The mixture was stirred for one hour at room temperature. Subsequently, aqueous saturated ammonium chloride solution was added to the reaction mixture for separation into a methylene chloride layer (200 mL) and an aqueous layer (200 mL). The organic layer was dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by means of silica gel column flash chromatography (hexane/ethyl acetate=99/1), to thereby afford 2.98 g (7.07 mmol) of 15-bromo-1-(t-butyldimethylsiloxy)pentadecane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235700B2
Source datasetuspto-grants-2007_06
ORD IDord-878b5950446146fa8720cc053302e1db
Source noteuspto-grants-2007_06