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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583373Generated: October 30, 2026

Carbon Dioxide → HCID 20260933, compound

https://huagongshe.com/reaction/1583373

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 1.55M 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 minues 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 2N 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 numberUS04551468
Source datasetuspto-grants-1985_11
ORD IDord-b10880e73b6d492dae6a53233143de33
Source noteuspto-grants-1985_11