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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045349Generated: October 31, 2026

Ethanol → HCID 56640672, compound

https://huagongshe.com/reaction/1045349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTosylmethyl isocyanideHCID 161915—
ReactantSpiro[5.5]undecan-3-oneHCID 574172—
ReactantPotassium tert-butoxideHCID 23665647—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 56640672HCID 5664067272.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of spiro[5.5]undecan-3-one (1.66 g, 10 mmol) and tosylmethylisocyanide (2.54 g, 13 mmol) in DME (50 ml) and abs. EtOH (1 ml) was added KOtBu (2.69 g, 24 mmol) portionwise during 0.5 hr at −10° C. After addition, the reaction mixture was stirred at 0° C. for 1 hr then 2 hr at ambient temperature. Solvent was removed in vacuo and the resulting residue was extracted with diethyl ether (50 ml×3) and the combined organic layer was washed with water (50 ml×3). The organic layer was dried with anhydrous MgSO4, concentrated under reduced pressure and purified by flash column chromatography (50%-100% CH2Cl2/Hexane) to give the nitrile as colorless solid (1.28 g, 72% Yield). 1H-NMR (360 MHz, CDCl3) δ 2.58-2.53 (m, 1H), 1.83-1.70 (m, 4H), 1.63-1.58 (m, 2H), 1.40-1.26 (m, 8H), 1.28-1.20 (m, 4H); 13C-NMR (90 MHz, CDCl3) δ 122.79, 34.41, 31.88, 28.37, 26.88, 24.73, 21.64, 21.55; ESI-MS: Calculated for C12H19N (M+H)+178.3. Found: 178.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569284B2
Source datasetuspto-grants-2013_10
ORD IDord-7d9cad20f425467090ca1192e6afb2a8
Source noteuspto-grants-2013_10