HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852476Generated: October 27, 2026
p-Toluenesulphonyl cyanide → 8-Oxospiro[4.5]decane-7-carbonitrile
https://huagongshe.com/reaction/1852476
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulphonyl cyanide | HCID 87946 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Spiro(4.5)decan-8-one | HCID 14626805 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-Oxospiro[4.5]decane-7-carbonitrile | HCID 86731013 | — |
Reaction Steps
LDA (1.83 mL, 3.66 mmol, 2.0 M in hexanes) was combined with THF (3.2 mL) and cooled to −78° C. To this mixture was added a solution of spiro[4.5]decan-8-one (0.50 g, 3.3 mmol) in THF (3.2 mL). The resulting mixture was stirred at −78° C. for 20 mins then taken up in a syringe and added to a mixture of tosyl cyanide (0.59 g, 3.3 mmol) in THF (3.2 mL) at −78° C. The reaction mixture was allowed to stir at −78° C. for 45 mins then quenched with 0.5M NaOH and extracted with EtOAc (2×). The combined organic extracts were washed with 1N aqueous HCl, brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The crude residue was purified by MPLC on silica gel (using a gradient elution of 0-50% EtOAc/hexanes). Desired fractions were identified, combined and concentrated in vacuo to afford the title compound. The residue was carried forward without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962608B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-b2522bd082f24ec79461117fe80458d7 |
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| Source note | uspto-grants-2015_02 |
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