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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648052Generated: October 29, 2026

Carbon Dioxide → HCID 20260933, compound

https://huagongshe.com/reaction/648052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDiisopropylamineHCID 7912—
ReactantHCID 20260910HCID 20260910—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductHCID 20260933HCID 20260933—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyl lithium (0.65 ml. of 1.55 M solution in hexane) was added dropwise to a stirred mixture of diisopropylamine (0.10 g.) and potassium t-butoxide (0.11 g.) in dry ether (10 ml.) at -78° C. under an atmosphere of dry nitrogen. The mixture was stirred at -78° C. for 45 minutes and then a solution of 3-methyl-6-(3-pyridylmethyl)benzo[b]thiophene (0.20 g.) in dry ether (5 ml.) was added. The solution was stirred at -78° C. for 45 minutes and then an excess of crushed solid carbon dioxide was added. When all the carbon dioxide had evaporated, water (5 ml.) was added and the mixture was shaken. The aqueous layer was then separated and washed with ether. It was then acidified with acetic acid and the solid was filtered off and dissolved in 2 N sodium hydroxide. The solution was decolorized by warming with charcoal and then filtered. Acidification of the filtrate with acetic acid gave a solid which was filtered off, washed with water and dried to give 3-methyl-6-(3-pyridylmethyl)-benzo[b]thiophene-2-carboxylic acid (0.10 g.), m.p. 250°-252° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04410539
Source datasetuspto-grants-1983_10
ORD IDord-b951f7061450458eba7a7b517a19e550
Source noteuspto-grants-1983_10