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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874993Generated: October 30, 2026

Hydrochloric Acid → HCID 68483604, compound

https://huagongshe.com/reaction/1874993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Methyl-1-buteneHCID 11240—
ReactantSodium Phosphate, Monobasic, MonohydrateHCID 516949—
Reactantethyl 5-formyl-3-methyl-1H-pyrrole-2-carboxylateHCID 1113514—
ReactantSodium ChloriteHCID 23668197—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventEthyl AcetateHCID 8857—
ProductHCID 68483604HCID 6848360472%

Reaction Steps

To a solution of ethyl 5-formyl-3-methyl-1H-pyrrole-2-carboxylate (0.25 g, 1.38 mmol) in t-BuOH (50 mL) was added 2-methylbutene as a 2M solution (24 mL, 48.3 mmol). In a separate flask sodium dihydrogen phosphate monohydrate (1.3 g, 9.42 mmol) and sodium chlorite (1.1 g, 12.2 mmol) were dissolved in water (30 mL). The aqueous solution was added to the alcoholic reaction mixture dropwise and stirred for 3 h. The solution was acidified with aqueous 1N HCl to a pH ˜4 and EtOAc (100 mL) added. The layers were separated, the aqueous layer extracted with EtOAc (5×25 mL), the organic layers combined, dried over sodium sulfate, filtered and the volume reduced (˜50 mL). Ethyl acetate (100 mL) was added and the solution extracted with sat. sodium bicarbonate (5×25 mL), the aqueous layers combined, acidified with 1N HCl to pH˜4-5, saturated with NaCl and extracted with EtOAc (5×25 mL). The organic layers were combined, dried over sodium sulfate, filtered and evaporated to afford 5-[(ethyloxy)carbonyl]-4-methyl-1H-pyrrole-2-carboxylic acid (0.196 g, 72%) as a white solid along with 3-chloro-5-[(ethyloxy)carbonyl]-4-methyl-1H-pyrrole-2-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-68b8cc9c16234665ba8eaf3ec24b5794
Source noteuspto-grants-2012_11