HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711972Generated: October 29, 2026
Sodium Cyanide → HCID 178453919, compound
https://huagongshe.com/reaction/711972
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | HCID 178453973 | HCID 178453973 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 178453919 | HCID 178453919 | — |
Reaction Steps
A mixture of {trans-4-[(tert-butoxycarbonyl)amino]cyclohexyl}methyl methanesulfonate (1.48 g, 4.81 mmol) and sodium cyanide (0.46 g, 9.4 mmol) in dimethyl sulfoxide (20 mL) was stirred at 90° C. for 4 h. After cooling, the mixture was partitioned between EtOAc and brine. The organic layer was washed with water, concentrated and purified on silica gel (eluting with 50% EtOAc in hexanes) to give tert-butyl [trans-4-(cyanomethyl)cyclohexyl]carbamate. LCMS calculated for C13H22N2O2Na (M+Na)+: m/z=261.2. Found: 261.1. A solution of the Boc-protected intermediate in methylene chloride (20 mL) was treated with trifluoroacetic acid (3 mL, 40 mmol) and the resulting mixture was stirred at room temperature for 2 h, then concentrated to give the desired product as TFA salt. LCMS calculated for C8H15N2 (M+H)+: m/z=139.1. Found: 139.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181271B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-6a559a3a26634259bfad1dfdc7492f70 |
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| Source note | uspto-grants-2015_11 |
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