HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181590Generated: October 26, 2026
Potassium Phosphate, Tribasic → Methyl 6-[2-[(1R)-1-(((2R)-oxiranyl)methoxy)ethyl]phenyl]hexanoate
https://huagongshe.com/reaction/1181590
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Methyl 5-Hexenoate | HCID 520082 | — |
| Reactant | (2R)-2-[[(1R)-1-(2-bromophenyl)ethoxy]methyl]oxirane | HCID 58981243 | — |
| Reactant | HCID 178419114 | HCID 178419114 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 6-[2-[(1R)-1-(((2R)-oxiranyl)methoxy)ethyl]phenyl]hexanoate | HCID 58662604 | 49.2% |
Reaction Steps
To methyl 5-hexenoate (608 mg) was added 0.5 M 9-bora bicyclo[3.3.1]nonane-tetrahydrofuran solution (9.5 ml) under ice-cooling and the mixture was stirred overnight at room temperature. The reaction mixture was added dropwise to a suspension of tetrahydrofuran (10 ml), (2R)-2-[[(1R)-1-(2-bromophenyl)ethoxy]methyl]oxirane (1.06 g) obtained in Example 1, Step 1, tri-potassium phosphate (1.32 g), [bis(diphenylphosphino)ferrocene]dichloropalladium(II) complex with dichloromethane (170 mg) and the mixture was heated under reflux for 7 hr. The reaction mixture was cooled to room temperature, water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=7:1) to give the title compound (621 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07285572B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-ea31a43bbcec4246a108e9f0af8137d4 |
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| Source note | uspto-grants-2007_10 |
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