HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → (5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl) acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 6-(Bromomethyl)-1,1,4,4-Tetramethyl-1,2,3,4-Tetrahydronaphthalene | HCID 2735597 | — |
| Catalyst | Tetraethylammonium cyanide | HCID 3014735 | — |
| Product | (5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl) acetonitrile | HCID 18177926 | 78% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06005007 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-4b26621781d34666b8fa0406b0e03f57 |
| Source note | uspto-grants-1999_12 |