HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl 4-(hydroxymethyl)-1,2,5-trimethylpyrrole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 4-formyl-1,2,5-trimethyl-1H-pyrrole-3-carboxylate | HCID 13425563 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl 4-(hydroxymethyl)-1,2,5-trimethylpyrrole-3-carboxylate | HCID 13051083 | — |
Reaction Steps
To a suspension of 10.9 g of ethyl 4-formyl-1,2,5-trimethylpyrrole-3-carboxylate in 40 ml of methanol is added dropwise under nitrogen 5.6 g of sodium borohydride in methanol while maintaining the reaction temperature below 50° C. after total addition the reaction mixture is stirred at ambient temperature for 4 hours, then 90 ml of water introduced and the reaction mixture saturated with potassium carbonate and extracted with ether. The combined ether extracts are dried and concentrated in vacuo leaving a yellow solid which is recrystallized from cyclohexane to give ethyl 4-(hydroxymethyl)-1,2,5-trimethylpyrrole-3-carboxylate, mp 184°-186° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04101559 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-4100ff82fd5e43d8a8cad61ca321a35c |
| Source note | uspto-grants-1978_07 |