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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349056Generated: October 25, 2026

Carbon Dioxide → 1-Butylisoquinoline-7-carboxylic acid

https://huagongshe.com/reaction/349056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant7-Bromo-1-butylisoquinolineHCID 21085995—
ReactantCID 53628100HCID 178418400—
SolventDiethyl EtherHCID 3283—
Product1-Butylisoquinoline-7-carboxylic acidHCID 21085177—

Reaction Steps

To a −60° C. solution of 7-bromo-1-butylisoquinoline prepared in step 1 (940 mg, 3.55 mmol) in diethyl ether (15 mL) was added sec-butyl lithium (3.0 mL, 1.3 M cyclohexanes, 3.90 mmol) to yield a dark green solution. The reaction mixture was stirred at −60° C. for an additional 15 minutes at which time carbon dioxide gas was bubbled through the solution for 20 minutes with the aid of a gas dispersion tube. The resulting solution was then allowed to warm to room temperature and concentrated under reduced pressure to yield a pink solid. The residue was partitioned between ethyl acetate and water and then acidified to pH 7 with 1 N hydrochloric acid. The aqueous phase was extracted again with ethyl acetate and the combined organic phases were washed with saturated sodium chloride, dried (sodium sulfate), filtered, and concentrated to yield 1-butylisoquinoline-7-carboxylic acid (299 mg). ESI MS m/z 230 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-885ba77874264456a2ada432f92109f6
Source noteuspto-grants-2007_02