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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920920Generated: November 1, 2026

Hydrochloric Acid → 8-Chloro-2-(2-(quinolin-2-YL)ethyl)phthalazin-1(2H)-one

https://huagongshe.com/reaction/920920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriphenylphosphineHCID 11776—
Reactant2-QuinolineethanolHCID 70532—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant8-Chloro-1(2H)-phthalazinoneHCID 71307662—
SolventTetrahydrofuranHCID 8028—
Product8-Chloro-2-(2-(quinolin-2-YL)ethyl)phthalazin-1(2H)-oneHCID 71743639—

Reaction Steps

To a solution of triphenylphosphine (9.00 g, 34.3 mmol) in THF (100 mL), DEAD (5.44 mL, 34.3 mmol) was added at 0° C. After stirring for 15 min, 2-(quinolin-2-yl)ethanol from Example a1 (2.97 g, 17.17 mmol) was added. After another 15 min, 8-chlorophthalazin-1(2H)-one (3.1 g, 17.17 mmol) was added. The mixture was stirred overnight at room temperature; LC-MS indicated complete conversion to the product. 1 N HCl was added (pH=4). The mixture was extracted with EtOAc (3×50 mL), the EtOAc layers were discarded. The aqueous layer was neutralized by aq.NaHCO3 and extracted with ethyl acetate (3×500 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product was suspended in EtOAc. The solid was filtered through a Büchner funnel. The purity of the title product was 95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273068B2
Source datasetuspto-grants-2016_03
ORD IDord-a7ca25ba64f14cc09726916b3f7c2876
Source noteuspto-grants-2016_03