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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508987Generated: October 30, 2026

Phosphorus trichloride → 4-chloro-2-(cyclopentyloxy)-6,7-dihydro-5H-cyclopenta[b]pyridine

https://huagongshe.com/reaction/1508987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus trichlorideHCID 24387—
Reactant4-chloro-2-(cyclopentyloxy)-6,7-dihydro-5H-cyclopenta[b]pyridine 1-oxideHCID 90112547—
SolventDichloromethaneHCID 6344—
Product4-chloro-2-(cyclopentyloxy)-6,7-dihydro-5H-cyclopenta[b]pyridineHCID 9033862625%

Reaction Steps

To a solution of crude 4-chloro-2-(cyclopentyloxy)-6,7-dihydro-5H-cyclopenta[b]pyridine 1-oxide (0.49 mmol) in methylene chloride (5 mL) was added phosphorous trichloride (0.100 g, 0.74 mmol). The mixture stirred at rt for 2 h. After this time, the mixture was quenched with a saturated solution of NaHCO3 and extracted with methylene chloride. The organic layer was dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was purified by column chromatography (silica, hexanes/ethyl acetate) to afford the title compound (0.029 g, 25% over two steps) as a clear oil. MW=237.73. 1H NMR (CDCl3, 300 MHz) δ 6.45 (s, 1H), 5.34-5.26 (m, 1H), 3.01-2.84 (m, 4H), 2.11 (quip; J=7.5 Hz, 2H), 2.00-1.57 (m, 8H); APCI MS m/z 238 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-9f6458f60f504c02aea840c48f69e713
Source noteuspto-grants-2015_12