Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | HCID 87332210 | HCID 87332210 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 67268225 | HCID 67268225 | — |
Reaction Steps
To the crude product, (S)-toluene-4-sulfonic acid 2-cyclohexyl-pent-4-enyl ester, in DMSO (40 mL) was added NaCN, and the resulting mixture was heated at 90° C. for 1.5 h. The reaction mixture was cooled to room temperature and treated with H2O (20 mL). The reaction mixture was then extracted with diethylether (3×25 mL), dried (MgSO4) and concentrated in vacuo to yield a residue which was purified by Kugelrohr distillation (0.19 mm Hg, 80-90° C.) to yield (R)-3-cyclohexyl-hex-5-enenitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868022B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-93080c8f1d5a4e80a30959e829576f96 |
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| Source note | uspto-grants-2011_01 |
|---|