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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356785Generated: October 31, 2026

Carbon Dioxide → HCID 18509425, compound

https://huagongshe.com/reaction/1356785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDimethylformamideHCID 6228—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 18509436HCID 18509436—
ReactantButyllithiumHCID 178418339—
SolventAcetoneHCID 180—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18509425HCID 1850942576.9%

Reaction Steps

Compound 7 (1.64 g: 5.12 mmol) was dissolved in tetrahydrofuran (20 ml), and the solution was cooled to −75° C. by use of a mixture of dry ice and acetone solvent under nitrogen atmosphere. n-butyl lithium in n-hexane (1.56 M: 3.3 ml; 5.12 mmol) was slowly added dropwise to the mixture, and the resultant mixture was stirred for 15 minutes. Subsequently, N,N-dimethylformamide (0.56 g; 7.68 mmol) was added dropwise to the mixture, and the resultant mixture was gradually brought to room temperature. Saturated aqueous ammonium chloride solution was added dropwise to the mixture, and the reaction was stopped, followed by extraction with ether (100 ml). The organic layer was washed with saturated aqueous sodium bicarbonate solution and with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=10:1), to thereby yield 1.06 g of the target compound (yield: 76.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586633B1
Source datasetuspto-grants-2003_07
ORD IDord-d84b1ce2cdd74c3cb4e5d7710e2838ff
Source noteuspto-grants-2003_07