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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 7-Bromo-1-butylisoquinoline | HCID 21085995 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Butylisoquinoline-7-carboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07176242B2 |
|---|
| Source dataset | uspto-grants-2007_02 |
|---|
| ORD ID | ord-885ba77874264456a2ada432f92109f6 |
|---|
| Source note | uspto-grants-2007_02 |
|---|