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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612735Generated: October 26, 2026

Acetonitrile → (5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl) acetonitrile

https://huagongshe.com/reaction/612735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantEthyl AcetateHCID 8857—
Reactant6-(Bromomethyl)-1,1,4,4-Tetramethyl-1,2,3,4-TetrahydronaphthaleneHCID 2735597—
CatalystTetraethylammonium cyanideHCID 3014735—
Product(5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl) acetonitrileHCID 1817792678%

Reaction Steps

To a solution of (5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl) bromomethane (21) (100 mg, 0.44 mmol) in acetonitrile (2 mL) was added tetraethylammonium cyanide (83 mg, 0.53 mmol). The resulting golden yellow solution was stirred at rt overnight. The solvent was removed in vacuo and to give a residue that was subjected to chromatograpy (10% EtOAc/90% hexane) to give 59 mg (78%) of (5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl) acetonitrile (22). 1H NMR (400 MHz, CDCl3) δ7.31 (d, J=8.2 Hz, 1H, aromatic), 7.23 (d, J=1.8 Hz, 1H, aromatic), 7.08 (dd, J=8.0 and 1.8 Hz, 1H, aromatic), 3.69 (s, 2H, CH2), 1.69 (s, 4H, 2CH2), 1.28 (s, 6H, 2CH3), (s, 6H, 2CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06005007
Source datasetuspto-grants-1999_12
ORD IDord-4b26621781d34666b8fa0406b0e03f57
Source noteuspto-grants-1999_12