HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363559Generated: October 29, 2026
{[1-(3-Azidopropyl)cyclohexyl]oxy}(tert-butyl)dimethylsilane → HCID 57515400, compound
https://huagongshe.com/reaction/1363559
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | {[1-(3-Azidopropyl)cyclohexyl]oxy}(tert-butyl)dimethylsilane | HCID 57457817 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57515400 | HCID 57515400 | 102.1% |
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 1 d, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884207B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-a4e9082c2a484beb8852216068079189 |
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| Source note | uspto-grants-2011_02 |
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