HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377094Generated: October 26, 2026
Hydrochloric Acid → HCID 178453601, compound
https://huagongshe.com/reaction/377094
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 178453600 | HCID 178453600 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178453601 | HCID 178453601 | 76% |
Reaction Steps
Ethanol (40 mL) was added to N-tert-butoxycarbonyl-trans-4-(aminomethyl)cyclohexanemethyl azide (1.79 g, 6.67 mmol.) and 5% palladium on carbon (270 mg, 0.15 wt. %) under nitrogen. The reaction mixture was stirred under hydrogen at atmospheric pressure for 6 hours at 23° C. The black suspension was filtered and the filtrate concentrated to give N-tert-butoxycarbonyl-trans-1,4-cyclohexane bis(methylamine) as a yellow oil. The crude amine was taken up into methanol (2.0 mL) followed by addition of hydrogen chloride in dioxane (4.0M, 2.0 mL, 8.0 mmol.) and ethyl ether (25 mL). The resulting precipitate was collected by filtration to give N-tert-butoxycarbonyl-trans-1,4-cyclohexanebis(methylamine)hydrochloride (1.42 g, 76% yield) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06022969 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-b262249441f94a74854f1791fa1b173a |
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| Source note | uspto-grants-2000_02 |
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