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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866770Generated: October 30, 2026

Water → Ethyl 4-(hydroxymethyl)-1,2,5-trimethylpyrrole-3-carboxylate

https://huagongshe.com/reaction/866770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 4-formyl-1,2,5-trimethyl-1H-pyrrole-3-carboxylateHCID 13425563—
SolventMethanolHCID 887—
ProductEthyl 4-(hydroxymethyl)-1,2,5-trimethylpyrrole-3-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04101559
Source datasetuspto-grants-1978_07
ORD IDord-4100ff82fd5e43d8a8cad61ca321a35c
Source noteuspto-grants-1978_07