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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601792Generated: October 29, 2026

Methyl (E)-5-(3-(tert-butoxy)-3-oxoprop-1-en-1-yl)-1H-pyrrole-2-carboxylate → methyl 5-(3-tert-butoxy-3-oxopropyl)-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/601792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl (E)-5-(3-(tert-butoxy)-3-oxoprop-1-en-1-yl)-1H-pyrrole-2-carboxylateHCID 66873605—
ReactantMethyl (Z)-5-(3-(tert-butoxy)-3-oxoprop-1-en-1-yl)-1H-pyrrole-2-carboxylateHCID 66873748—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Productmethyl 5-(3-tert-butoxy-3-oxopropyl)-1H-pyrrole-2-carboxylateHCID 66873239100%

Reaction Steps

To a solution of (z)-methyl 5-(3-tert-butoxy-3-oxoprop-1-enyl)-1H-pyrrole-2-carboxylate or (E)-methyl 5-(3-tert-butoxy-3-oxoprop-1-enyl)-1H-pyrrole-2-carboxylate (13.6 g, 54.1 mmol, 2 equal batches) in EtOAc (200 mL) under nitrogen was added 10% Pd/C. The flask was flushed with hydrogen three times before allowing the reaction to stir under hydrogen for about 18 h. The catalyst was filtered off using Celite and the filtrate was concentrated to give 27.4 g methyl 5-(3-tert-butoxy-3-oxopropyl)-1H-pyrrole-2-carboxylate as a white solid (100%) for each stereoisomer. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.46 (s, 9H), 2.54-2.59 (m, 2H), 2.90 (t, J=6.83 Hz, 2H), 3.83 (s, 3H), 5.97 (dd, J=3.49, 2.86 Hz, 1H), 6.81 (dd, J=3.61, 2.59 Hz, 1H), 9.30 (br s, 1H); LCMS-MS (ESI+) 197.86 (M-isobutylene).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902252B2
Source datasetuspto-grants-2011_03
ORD IDord-5aa934da671b4e32946a15d94cfa859a
Source noteuspto-grants-2011_03