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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379081Generated: October 25, 2026

Carbon Dioxide → Propiolic Acid

https://huagongshe.com/reaction/1379081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantChloromethyl Methyl EtherHCID 7864—
Reactant5-(Bromomethyl)-3-methoxy-1,2-oxazoleHCID 10845405—
Reactant3-Diphenylmethoxy-4-iodomethyl-1,2,5-thiadiazoleHCID 22906284—
ReactantHCID 178462446HCID 178462446—
SolventTetrahydrofuranHCID 8028—
ProductPropiolic AcidHCID 10110—
ProductHCID 178462446HCID 178462446—

Reaction Steps

Dibromoolefin intermediate XIX is then converted to ethynyl intermediate XX. Treatment of the dibromoolefin intermediate with about two equivalents of n-butyllithium produces the lithium acetylide XX, wherein R13 is Li. This transformation is typically carried out in a polar organic solvent, such as tetrahydrofuran, at a temperature of about -78° C. to about 25° C. The lithium acetylide is reacted with electrophiles, such as methoxymethyl chloride, 5-bromomethyl-3-methoxyisoxazole, 3-diphenylmethoxy-4-iodomethyl-1,2,5-thiadiazole, carbon dioxide, tetrazole disulfide, and the like, to prepare the formula I compounds. In a typical example, the lithium acetylide is treated with solid CO2 at a temperature of about -78° C. to about -60° C. to produce propargylic acid intermediate XX wherein R13 is CO2H. This compound may be further modified as described herein.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670516
Source datasetuspto-grants-1997_09
ORD IDord-0959af75a1d443efa21b0b9362963da6
Source noteuspto-grants-1997_09