HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 20285713, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20285662 | HCID 20285662 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20285713 | HCID 20285713 | — |
Reaction Steps
15.0 G. of 2,4-dimethyl-5-(methylthio)thiophene-3-carboxaldehyde was dissolved in 150 ml. of dry ethanol with stirring at 20° C. 0.8 G. of sodium borohydride was added and the mixture was stirred for 30 minutes, then poured into ice water and extracted with ethyl ether. The combined ether extracts were washed with a solution of 5% sodium carbonate and saturated sodium chloride solution, dried over sodium sulfate, filtered, and evaporated to yield 2,4-dimethyl-3-hydroxymethyl-5-(methylthio)thiophene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04116975 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-61b81288a7f1457880e4a841efc915b4 |
| Source note | uspto-grants-1978_09 |