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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465398Generated: October 26, 2026

Methyl 4-tridecanoylpyrrole-2-carboxylate → Methyl 4-tridecylpyrrole-2-carboxylate

https://huagongshe.com/reaction/465398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-tridecanoylpyrrole-2-carboxylateHCID 15023257—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductMethyl 4-tridecylpyrrole-2-carboxylateHCID 1502327491.8%

Reaction Conditions

Temperature30 °C

Reaction Steps

Into a mixture of 150 ml of Raney nickel (activated type, produced by Aldrich Co.), which had been washed with water and then ethanol, and 750 ml of ethanol, was added 15.06 g (37.9 mmol) of dithioethyleneketal of methyl 4-tridecanoylpyrrole-2-carboxylate obtained in Synthesis Example 2. The mixture was refluxed for 30 minutes and cooled to about 30° C. After removing Raney nickel, the mixture was evaporated. The residue was recrystallized from ethanol to obtain 10.70 g of methyl 4-tridecylpyrrole-2-carboxylate as white crystals. The yield was 91.8% and the melting point was 80° to 82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05153217
Source datasetuspto-grants-1992_10
ORD IDord-e0c14aff3eaa4a4dbb4c55657e53dbab
Source noteuspto-grants-1992_10