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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541180Generated: November 1, 2026

Phosphorus oxychloride → Tert-butyl 4-(4-cyanophenyl)-3,6-dihydropyridine-1(2h)-carboxylate

https://huagongshe.com/reaction/541180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantTert-butyl 4-(4-cyanophenyl)-4-hydroxypiperidine-1-carboxylateHCID 59003435—
SolventPyridineHCID 1049—
ProductTert-butyl 4-(4-cyanophenyl)-3,6-dihydropyridine-1(2h)-carboxylateHCID 1128911274.5%

Reaction Steps

Into a round-bottom flask, was placed a solution of tert-butyl 4-(4-cyanophenyl)-4-hydroxypiperidine-1-carboxylate (compound 1.2, 2 g, 6.61 mmol, 1.00 equiv) in pyridine (40 mL). POCl3 (10.16 g, 66.26 mmol, 10.02 equiv) was carefully added. The resulting mixture was stirred under nitrogen overnight at room temperature and then concentrated under vacuum. The residue was taken up in 20 mL of DCM, washed with 2×20 mL of sodium bicarbonate (aq), dried (Na2SO4), and concentrated under reduced pressure. The residue was purified using silica gel column chromatography with PE/EtOAc (100:1-30:1) as eluent to yield 1.4 g (74%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-1577c826758d43b5879d3577b9cf0bc6
Source noteuspto-grants-2014_10