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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601895Generated: October 30, 2026

methyl 4-(3-tert-butoxy-3-oxoprop-1-enyl)-1H-pyrrole-2-carboxylate → methyl 4-(3-tert-butoxy-3-oxopropyl)-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/601895

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 4-(3-tert-butoxy-3-oxoprop-1-enyl)-1H-pyrrole-2-carboxylateHCID 66874596—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Productmethyl 4-(3-tert-butoxy-3-oxopropyl)-1H-pyrrole-2-carboxylateHCID 59180142100.2%

Reaction Steps

To a solution of methyl 4-(3-tert-butoxy-3-oxoprop-1-enyl)-1H-pyrrole-2-carboxylate (2.0 g, 7.96 mmol) in EtOAc (20 mL) under nitrogen was added 10% Pd/C. The flask was evacuated and refilled with hydrogen three times. The reaction mixture was stirred for 2 h. The catalyst was removed by filtration through Celite and the filtrate was concentrated to give methyl 4-(3-tert-butoxy-3-oxopropyl)-1H-pyrrole-2-carboxylate as a white solid (2.02 g, 100%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.43 (s, 9H), 2.48 (t, J=7.59 Hz, 2H), 2.77 (t, J=7.54 Hz, 2H), 3.84 (s, 3H), 6.77 (dd, J=2.37, 1.93 Hz, 2H), 930 (br s, 1H); LCMS-MS (ESI+) 198.2 (M-isobutylene).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902252B2
Source datasetuspto-grants-2011_03
ORD IDord-dbf7eb177f1d49ad83bb44ae8c851ebb
Source noteuspto-grants-2011_03