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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437473Generated: October 30, 2026

Carbon Dioxide → HCID 13478464, compound

https://huagongshe.com/reaction/437473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant5,6,7,8-Tetrahydro-3,7,7-trimethylquinolineHCID 12278205—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductHCID 13478464HCID 1347846410%

Reaction Steps

3,7,7-Trimethyl-5,6,7,8-tetrahydroquinoline (17.5 g., 0.1 m) was dissolved in dry ether (200 ml.) and treated with a solution of n-butyl lithium in hexane (15% solution, 56 ml.) under nitrogen. The reaction mixture was allowed to stand at room temperature for 30 minutes and then treated with CO2 gas until the intense red colour was discharged. The solvent was removed and the residual oily solid dissolved in water (20 ml.) then extracted with ether (3 × 50 ml.). The ethereal extracts were retained to recover unreacted starting material. The aqueous solution was evaporated to dryness, the residue treated with methanol previously saturated with dry HCl (100 ml.) and the solution allowed to stand at room temperature for 8 hours. The solvent was removed and the residual oil dissolved in water (50 ml.) and extracted with ether (3 × 50 ml.) and the extracts discarded. The aqueous solution was adjusted to pH 9.0 with sodium carbonate and extracted with ether (3 × 50 ml.). The combined extracts were dried and evaporated in vacuo to give the title compound as a pale yellow oil (1.8 g., 10%) I.R. Spectrum ν maxfilm 1748, 1570, 1460, 1160, 1030 cm-1. GLC : RT =3.1/2 min. (F11, 2% OV17, T = 150°).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031102
Source datasetuspto-grants-1977_06
ORD IDord-66d17c4f6c2d421592b8209d8d03c167
Source noteuspto-grants-1977_06