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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44723Generated: October 29, 2026

Sodium Azide → {[1-(3-Azidopropyl)cyclohexyl]oxy}(tert-butyl)dimethylsilane

https://huagongshe.com/reaction/44723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactant3-(1-{[Tert-butyl(dimethyl)silyl]oxy}cyclohexyl)propyl methanesulfonateHCID 57457816—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product{[1-(3-Azidopropyl)cyclohexyl]oxy}(tert-butyl)dimethylsilaneHCID 5745781795.2%

Reaction Steps

Sodium azide (1.78 g, 27.4 mmol) was added to a solution of 3-(1-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)propyl methanesulfonate (prepared as described in Part D, 24.9 mmol) in dimethylformamide (100 mL). The reaction mixture was stirred for 2.5 d and additional sodium azide (160 mg) was added. The mixture was stirred an additional 1d, then was diluted with diethyl ether (250 mL) and washed with water (3×75 mL). The combined aqueous layers were back-extracted with diethyl ether (50 mL). The combined organic layers were washed with brine (100 mL), dried over MgSO4, filtered, and concentrated to afford {[1-(3-azidopropyl)cyclohexyl]oxy}(tert-butyl)dimethylsilane (7.05 g, 95% over two steps) as a pale yellow oil. A mixture of the {[1-(3-azidopropyl)cyclohexyl]oxy}(tert-butyl)dimethylsilane (7.05 g, 23.7 mmol) and 5% palladium on carbon (0.71 g) in ethanol (100 mL) was hydrogenated at 30 psi (2.1×105 Pa) for 4 h on a Parr apparatus. The reaction mixture was filtered through CELITE filter agent, which was rinsed afterwards with dichloromethane, and the filtrate was concentrated to give 3-(1-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)propan-1-amine as a pale yellow oil (6.57 g, 102%) that contained a trace amount of solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541438B2
Source datasetuspto-grants-2013_09
ORD IDord-f4dfc273a5344a92ad4c8a50e1d889f7
Source noteuspto-grants-2013_09