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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulphonyl cyanideHCID 87946—
ReactantLithium diisopropylamideHCID 2724682—
ReactantSpiro(4.5)decan-8-oneHCID 14626805—
SolventTetrahydrofuranHCID 8028—
Product8-Oxospiro[4.5]decane-7-carbonitrileHCID 86731013—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962608B2
Source datasetuspto-grants-2015_02
ORD IDord-b2522bd082f24ec79461117fe80458d7
Source noteuspto-grants-2015_02