HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-Hydroxymethyl-3,4,5-trimethyl-thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3,4,5-Trimethylthiophene-2-carbaldehyde | HCID 12875262 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Hydroxymethyl-3,4,5-trimethyl-thiophene | HCID 12875259 | — |
Reaction Steps
1.9 G. of 3,4,5-trimethyl-2-thiophenecarboxaldehyde were dissolved in 20 ml. of ethanol. The resulting solution was cooled to 0°-5° C. and 125 mg. of sodium borohydride were added in small portions. The resulting reaction mixture was stirred at room temperature for 3 hours, poured into ice water, extracted with ethyl acetate, dried with sodium sulfate, filtered and evaporated. The resulting crystalline 2-hydroxymethyl-3,4,5-trimethyl-thiophene had m.p. 45°-48° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04061656 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-65f8bdfdac0341e99807b4fb11bcb7cd |
| Source note | uspto-grants-1977_12 |