HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 12875271, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 63826-91-5 | HCID 12875269 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12875271 | HCID 12875271 | — |
Reaction Steps
11.8 G. of 4-bromo-3,5-dimethylthiophene-2-carboxaldehyde was dissolved in 250 ml. of dry ethanol and stirred at 20° C. 0.52 G. of sodium borohydride was added and the resulting solution 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 50% sodium carbonate and a saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated. Crystallization from cold hexane yielded 4-bromo-3,5-dimethyl-2-hydroxymethylthiophene, m.p. 85°-90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04061656 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-525686ed9fb049768afe683db547282e |
| Source note | uspto-grants-1977_12 |