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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647946Generated: November 2, 2026

Carbon Dioxide → HCID 9839090, compound

https://huagongshe.com/reaction/1647946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
ReactantMagnesiumHCID 5462224—
ReactantHCID 86748799HCID 86748799—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9839090HCID 983909061%

Reaction Steps

5.6 g of 1-[3-chloro-4-(2,2-ethylenedioxycyclohexane-1-yl methyl)phenyl]ethyl bromide were dissolved in 50 ml of tetrahydrofuran and added dropwise over one hour to 0.55 g of magnesium suspended in 10 ml of tetrahydrofuran, after which the whole was refluxed under agitation for three hours and cooled to produce a Grignard's reagent. The Grignard's reagent so produced was poured onto an excessive amount of solid carbon dioxide and allowed to stand still for 4 hours, after which the whole was acidified with diluted hydrochloric acid and extracted with 100 ml of ether. The extract obtained was concentrated to obtain a residue which was then incorporated with 25 ml of acetic acid and 10 ml of water and refluxed under agitation for two hours. After the end of the reaction, the reaction mixture was incorporated with 100 ml of water and extracted with 50 ml of ether. The extract obtained was washed with water, dried and freed of the solvent to obtain a residue which was then recrystallized from isopropyl ether thereby to obtain 2.7 g (yield 61%) of 2-[3-chloro-4-(2-oxocyclohexane-1-yl methyl)phenyl] propionic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434292
Source datasetuspto-grants-1995_07
ORD IDord-859c76ca6de1403794e950da892d5eac
Source noteuspto-grants-1995_07