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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037973Generated: November 1, 2026

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

https://huagongshe.com/reaction/1037973

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 numberUS08546588B2
Source datasetuspto-grants-2013_10
ORD IDord-b9090638e8ff4ceab73b9c219f3808ee
Source noteuspto-grants-2013_10