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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631885Generated: November 2, 2026

5-(4-Fluoro-benzyl)-3-methoxy-2-(2,4,6-trimethyl-phenyl)-cyclopent-2-enone → 4-(4-Fluoro-benzyl)-2-(2,4,6-trimethyl-phenyl)-cyclopentane-1,3-dione

https://huagongshe.com/reaction/1631885

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Fluoro-benzyl)-3-methoxy-2-(2,4,6-trimethyl-phenyl)-cyclopent-2-enoneHCID 66868234—
SolventAcetoneHCID 180—
SolventHydrochloric AcidHCID 313—
Product4-(4-Fluoro-benzyl)-2-(2,4,6-trimethyl-phenyl)-cyclopentane-1,3-dioneHCID 6686808695.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 5-(4-fluoro-benzyl)-3-methoxy-2-(2,4,6-trimethyl-phenyl)-cyclopent-2-enone (136 mg, 0.40 mmol) in acetone (2 ml) is added a 2N solution of hydrochloric acid (2 ml) and the resulting solution is heated to 40° C. by microwave irradiation for 30 minutes. The reaction mixture is diluted with 2N hydrochloric acid (25 ml), and extracted with ethyl acetate (2×25 ml). The combined organics are washed with brine (25 ml), dried over magnesium sulphate, filtered and concentrated in vacuo to give 4-(4-fluoro-benzyl)-2-(2,4,6-trimethyl-phenyl)-cyclopentane-1,3-dione (124 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791303B2
Source datasetuspto-grants-2014_07
ORD IDord-1529d5ab2a904ecf94937effc348343b
Source noteuspto-grants-2014_07