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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861776Generated: October 30, 2026

Methanol → methyl 4-iodo-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/861776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium MethoxideHCID 10942334—
Reactant2,2,2-trichloro-1-(4-iodo-1H-pyrrol-2-yl)ethan-1-oneHCID 11681602—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Productmethyl 4-iodo-1H-pyrrole-2-carboxylateHCID 11673249—

Reaction Steps

8.2 g (24 mmol) of 4-iodo-2-trichloroacetylpyrrole and 100 ml of methanol were introduced into a round-bottomed flask and 2 g (36 mmol) of sodium methoxide were added. Stirring was carried out at room temperature for four hours, the reaction mixture was evaporated to dryness and the residue obtained was taken up in water and ethyl ether. The organic phase was separated by settling, dried over magnesium sulfate and evaporated. The residue obtained was triturated in heptane and filtered. 4.9 g (81%) of the expected ester, with a melting point of 77°-78° C., were recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716624
Source datasetuspto-grants-1998_02
ORD IDord-cd9bccabfb254088b41bd21d166a2525
Source noteuspto-grants-1998_02