HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872095Generated: November 1, 2026
5-Methoxybicyclo[4.2.0]octa-1,3,5-trien-7-one → Bicyclo[4.2.0]octa-1,3,5-trien-7-ol, 5-methoxy-
https://huagongshe.com/reaction/1872095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Methoxybicyclo[4.2.0]octa-1,3,5-trien-7-one | HCID 2752744 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Bicyclo[4.2.0]octa-1,3,5-trien-7-ol, 5-methoxy- | HCID 10103323 | 67% |
Reaction Steps
13.21 g (0.35 mol) of sodium borohydride are added in small fractions to a solution, maintained at 0° C., of 42.8 g (0.29 mol) of 6-methoxybenzocyclobutan-1-one in 1.5 liters of methanol. The temperature is maintained at 0° C. for 2 hours. After returning to room temperature, the reaction mixture is evaporated to dryness and then taken up in water. The aqueous phase is extracted several times with ethyl acetate. The organic phases are combined, washed with brine, dried over MgSO4, filtered and evaporated to yield, after chromatography on silica, 29.2 g of the expected product in the form of a solid, the melting point of which is 71-73° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06107345 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-eb337e61c1ce4e36971446a5f7b74f13 |
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| Source note | uspto-grants-2000_08 |
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