HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 5-(Hydroxymethyl)furan-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 5-cyanofuran-2-carboxylate | HCID 13011707 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(Hydroxymethyl)furan-2-carbonitrile | HCID 3021406 | — |
Reaction Steps
A solution of the ester from step 1 (0.098 g, 0.652 mmol), in ethanol (2.5 ml) at 0° C. was treated with sodium borohydride (0.11 g, 2.936 mmol) and the reaction was stirred for 2 hrs. Saturated NH4Cl solution (1 ml) was added and the aqueous extracted with diethylether. The combined extracts were dried (MgSO4) and evaporated in vacuo. The residue was chromatographed (silica gel, diethylether) to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06077853 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-0f69dbcd0e5247d9b9ae3edacd9a6513 |
| Source note | uspto-grants-2000_06 |