Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588512Generated: October 30, 2026

Water → methyl 5-formyl-1-methyl-1H-pyrrole-3-carboxylate

https://huagongshe.com/reaction/588512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantMethyl 5-formylpyrrole-3-carboxylateHCID 579027—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Productmethyl 5-formyl-1-methyl-1H-pyrrole-3-carboxylateHCID 1417385580%

Reaction Steps

To a solution of methyl 5-formyl-1H-pyrrole-3-carboxylate (60.0 g, 0.360 mol) in DMF (60 mL) was added potassium tert-butoxide (72.0 g, 0.576 mol). After stirring at rt for 30 min, the mixture was cooled to 0° C. and methyl iodide (132 mL, 1.45 mol) was added. The solution was then stirred at rt overnight. Water was added to quench the reaction and the solution was extracted with DCM (3×200 mL). The combined organic phases were washed with brine (50 mL), dried (Na2SO4), and concentrated to give methyl 5-formyl-1-methyl-1H-pyrrole-3-carboxylate (45.0 g, 80%). 1H NMR (CDCl3, 400 MHz) δ 12.62 (s, 1H), 9.48 (s, 1H), 7.66 (s, 1H), 7.30 (s, 1H), 3.67 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227951B2
Source datasetuspto-grants-2016_01
ORD IDord-e89de35399924a51a8c87293ececb3a9
Source noteuspto-grants-2016_01