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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554059Generated: October 31, 2026

Carbon Dioxide → HCID 67121019, compound

https://huagongshe.com/reaction/554059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant1,2,3,4-TetrahydroquinolineHCID 69460—
ReactantTetramethyl cyclopentenoneHCID 130026774—
ReactantHCID 178418306HCID 178418306—
ReactantButyllithiumHCID 178418339—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67121019HCID 6712101941%

Reaction Conditions

Temperature-78 °C

Reaction Steps

957 mg (7.185 mmol) of 1,2,3,4-tetrahydroquinoline was dissolved in 10 ml of THF, and stirred at −78° C. for 30 minutes. 2.87m1 (7.185mmol) of nBuLi was added thereto using a syringe under a nitrogen atmosphere (yellow suspension). The mixture was sufficiently stirred for 3 hours, and the temperature was increased to −20° C. to eliminate the gas. The temperature was cooled again to −78° C. and CO2 was injected to the mixture (The color of the mixture turned to colorless white). The temperature was increased to −20° C. and the remaining CO2 was eliminated in vacuum for 1 hour. Then, 5.07 ml (8.622 mmol) of tert-butyllitium (BuLi) was added to the mixture (The color of the mixture turned to red). While the temperature was maintained at −20° C., the mixture was sufficiently stirred for 2 hours, and 26.1 ml (8.622 mmol) of 0.33 M CeCl3:2LiCl solution dissolved in THF and 1.182 g (8.622 mmol) of tetramethyl cyclopentenone were added to the mixture under a nitrogen atmosphere. While the temperature was gradually increased to room temperature, the solvents were eliminated by venting. Then, the mixture was titurated using pentane under a nitrogen atmosphere and filtered to obtain a white crystalline powder (41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048973B2
Source datasetuspto-grants-2011_11
ORD IDord-9ac8b71405c0429db68b1dd7572a36fe
Source noteuspto-grants-2011_11