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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Phenylethanol, (R)- | HCID 637516 | — |
| Reactant | 1-(4-Chlorophthalazin-1-yl)-7-methoxynaphthalen-2-ol | HCID 136343453 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Methoxy-1-[4-((R)-1-phenyl-ethoxy)-phthalazin-1-yl]-naphthalen-2-ol | HCID 136352503 | 86.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790882B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-984b8e45f7044bec9fc262c677bde064 |
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| Source note | uspto-grants-2010_09 |
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