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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711980Generated: October 25, 2026

Sodium hydride → 7-Methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-ol

https://huagongshe.com/reaction/1711980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-Phenylethanol, (R)-HCID 637516—
Reactant1-(4-Chlorophthalazin-1-yl)-7-methoxynaphthalen-2-olHCID 136343453—
SolventTetrahydrofuranHCID 8028—
Product7-Methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-olHCID 13635250386.7%

Reaction Steps

To a suspension of sodium hydride (0.80 g, 33 mmol) in tetrahydrofuran (80 ml) was added a solution of (R)-phenylethanol (2.0 g, 17 mmol) in tetrahydrofuran (3 ml) cautiously over 10 min at 23° C. The mixture was stirred for 15 min, then 1-(4-chlorophthalazin-1-yl)-7-methoxy-naphthalen-2-ol (5.1 g, 15 mmol) was added portionwise. The resulting red suspension was stirred for 20 hrs at 23° C., then the solvent was removed under reduced pressure. The residue was dissolved in dichloromethane and poured into brine. The organic layer was separated and the aqueous layer was extracted two times with dichloromethane. The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (hexane/EtOAc 4:1 to 1:1) to give 5.5 g (13 mmol) of the title compound as a 1:1 mixture of diastereomers, as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790882B2
Source datasetuspto-grants-2010_09
ORD IDord-984b8e45f7044bec9fc262c677bde064
Source noteuspto-grants-2010_09