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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662047Generated: October 29, 2026

Methanol → ethyl 5-hydroxymethyl-1,4-dimethyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/1662047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactantethyl 5-formyl-1,4-dimethyl-1H-pyrrole-2-carboxylateHCID 59454108—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Productethyl 5-hydroxymethyl-1,4-dimethyl-1H-pyrrole-2-carboxylateHCID 5945402566%

Reaction Steps

To a mixture of ethyl 5-formyl-1,4-dimethyl-1H-pyrrole-2-carboxylate (0.99 g) and methanol (10 ml) was added sodium borohydride (0.38 g) under ice-cooling, followed by stirring for 5 minutes under ice-cooling. To a reaction mixture was added a saturated aqueous ammonium chloride solution under ice-cooling, followed by stirring at room temperature for 0.5 hour. To the reaction mixture were added water and ethyl acetate, and the aqueous layer was separated and extracted with ethyl acetate. The organic layer was combined, washed with a saturated sodium bicarbonate solution and saturated brine in this order, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=4:1) to obtain ethyl 5-hydroxymethyl-1,4-dimethyl-1H-pyrrole-2-carboxylate (0.66 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030489B2
Source datasetuspto-grants-2011_10
ORD IDord-c7b63308f5d74e49b665a7c9fdaa6c1c
Source noteuspto-grants-2011_10