HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1-(2-Hydroxyethyl)-3,4-dihydro-1H-2-benzopyran-6-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-(6-Bromoisochroman-1-yl)ethanol | HCID 23288830 | — |
| Catalyst | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(2-Hydroxyethyl)-3,4-dihydro-1H-2-benzopyran-6-carbonitrile | HCID 23635693 | — |
Reaction Steps
2-(6-Bromo-3,4-dihydro-1H-2-benzopyran-1-yl)ethanol (1.3 g, 5.1 mmol), zinc cyanide (0.36 g, 3 mmol) and tetrakis(triphenylphosphine)palladium (0) (0.23 g, 0.20 mmol) were stirred in degassed DMF (20 mL) under nitrogen at reflux for 9 h. The reaction mixture was diluted with toluene and washed with 2M aqueous ammonia, the aqueous layer further extracted with ethyl acetate, then the combined organic extracts washed with brine. The organic extracts were dried (MgSO4), filtered and evaporated in vacuo. Purification by flash chromatography on silica, eluting with ethyl acetate/hexane (30:70 to 0:100), yielded the title compound as a light brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07335660B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-d64321dbd07445369983bdb99ac1efe6 |
| Source note | uspto-grants-2008_02 |