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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methoxybicyclo[4.2.0]octa-1,3,5-trien-7-oneHCID 2752744—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductBicyclo[4.2.0]octa-1,3,5-trien-7-ol, 5-methoxy-HCID 1010332367%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107345
Source datasetuspto-grants-2000_08
ORD IDord-eb337e61c1ce4e36971446a5f7b74f13
Source noteuspto-grants-2000_08