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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617499Generated: October 31, 2026

Carbon Dioxide → HCID 136166971, compound

https://huagongshe.com/reaction/1617499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHCID 136167038HCID 136167038—
SolventTetrahydrofuranHCID 8028—
ProductHCID 136166971HCID 13616697129%

Reaction Conditions

Temperature0 °C

Reaction Steps

At −78° C., to a solution of (E)-3-(3-bromo-phenyl)-3-phenyl-1-pyridin-4-yl-propan-1-one oxime (60 mg, example 12) in THF (1.5 mL) n-BuLi (1.6 M in hexane, 0.11 mL) was added dropwise. After stirring for 30 mins at that temperature carbon dioxide gas was bubbled into the solution for 5 min at −78° C. The reaction mixture was then warmed up to 0° C. and stirred for 15 min. The reaction was quenched by adding 1N aqueous KHSO4 solution, the phases were separated and the inorganic one was extracted with EtOAc (2×). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. Column chromatography on silica gel (CH2Cl2/MeOH 97:3) yielded 3-{3-[(E)-hydroxyimino]-1-phenyl-3-pyridin-4-yl-propyl}-benzoic acid (16 mg, 29%) as a yellow foam, MS (ESI+): m/z=347.1391 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765730B2
Source datasetuspto-grants-2014_07
ORD IDord-354810192c3048259a62b7987e19acb3
Source noteuspto-grants-2014_07