HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 3,4-Dihydro-2H-1-benzopyran-2-acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | HCID 9858183 | HCID 9858183 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3,4-Dihydro-2H-1-benzopyran-2-acetonitrile | HCID 14838441 | 58.2% |
Reaction Steps
10.6 g (0.216 mol) of sodium cyanide are added to a solution of 57.31 g (0.18 mol) of 2-(p-toluenesulphonyloxymethyl)chroman in 800 ml of absolute dimethylformamide and the whole is heated, while stirring, to 60°. After 10 hours, ice-water is added to the reaction mixture and extraction is carried out with diethyl ether. The combined ethereal phases are washed thoroughly with water, dried over sodium sulphate and concentrated by evaporation in vacuo. 30.0 g (96.2%) of crude product are obtained and are chromatographed on 1000 g of silica gel (0.040-0.063 mm) using toluene as the eluant. 18.16 g (58.2%) of 2-cyanomethylchroman are thus obtained in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05112855 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-3ea909180fe34d018a1a82128d6389f7 |
| Source note | uspto-grants-1992_05 |