HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiophenecarboxaldehyde → Thien-2-yl-hydroxyacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiophenecarboxaldehyde | HCID 7364 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | CID 6399220 | HCID 6399220 | — |
| Solvent | Water | HCID 962 | — |
| Product | Thien-2-yl-hydroxyacetonitrile | HCID 11469116 | 59.3% |
Reaction Steps
In this example 25.0 g of 2-formylthiophene was added to a stirred solution containing 10.93 g of sodium cyanide in 37 ml of water at room temperature. 63 ml of aqueous saturated sodium acid sulfite was then slowly added to the stirred mixture. During the addition of the sodium acid sulfite solution, small amounts (about 20 g) of ice were periodically added. The mixture was then stirred for another 15 minutes and extracted with ethyl ether. The ethyl ether extracts were combined, dried over magnesium sulfate and evaporated under vacuum affording 18.4 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04537623 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-dc8afed6f1e6470da0a6400d0a8f8159 |
| Source note | uspto-grants-1985_08 |