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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296843Generated: October 31, 2026

Hydrochloric Acid → HCID 12150310, compound

https://huagongshe.com/reaction/1296843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantTetrahydrofuranHCID 8028—
Reactant(4-Chlorophenyl) 2-pyridyl ketoneHCID 80594—
ReactantCinchonineHCID 90454—
ProductHCID 12150310HCID 1215031081%

Reaction Steps

Under argon atmosphere, cinchonine (440 mg, 1.0 mmol) was suspended in tetrahydrofuran (absolute, 2.0 mL), and to this suspension was added a Reformatsky reagent (0.5 M; 8.0 mL, 4.0 mmol) dropwise under ice-cooling. After stirring for 10 minutes, pyridine (0.30 mL, 2 mmol) was added thereto dropwise. After stirring for 20 minutes under ice-cooling, the mixture was cooled to −400° C. A solution of 2-(4-chlorobenzoyl)pyridine (218mg, 1.0 mmol) in tetrahydrofuran (absolute, 4.0 mL) was added dropwise over 10 minutes, and the mixture was stirred at −40° C. for 4 hours. To this reaction solution was added 1N HCl (20 mL), which was then extracted with ethyl acetate (20 mL×2). The extracted solution was washed successively with an aqueous saturated sodium bicarbonate solution and an aqueous saturated sodium chloride solution. After the organic layer was dried with sodium sulfate, the solvent was removed under reduced pressure. The residue was analyzed with high performance liquid chromatography. Consequently, the yield was 81% and the enantiomer excess was 91%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247732B2
Source datasetuspto-grants-2007_07
ORD IDord-81b73f2684994af5b0ce79ee7241efb1
Source noteuspto-grants-2007_07