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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 15-Bromopentadecan-1-ol | HCID 543850 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [(15-Bromopentadecyl)oxy](tert-butyl)dimethylsilane | HCID 23615174 | 94.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07235700B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-878b5950446146fa8720cc053302e1db |
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| Source note | uspto-grants-2007_06 |
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