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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196237Generated: October 31, 2026

Trifluoroacetic acid → HCID 67915874, compound

https://huagongshe.com/reaction/1196237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantN-Benzyl-1-butoxy-N-[(trimethylsilyl)methyl]methanamineHCID 11097910—
Reactant4,4-Bis(3-fluorophenyl)cyclohexenoneHCID 54307328—
SolventDichloromethaneHCID 6344—
ProductHCID 67915874HCID 67915874—

Reaction Steps

Trifluoroacetic acid (3 cc) is added to a solution of 4,4-bis(3-fluorophenyl)cyclohexenone (90.3 g) and N-butoxymethyl-N-(trimethylsilylmethyl)benzylamine (123 cc) in dry dichloromethane (1000 cc). The reaction mixture is brought to reflux, then stirred for 2 hours while allowing the temperature to return to 25° C. and for a further 15 minutes after the addition of potassium carbonate (60 g). After filtration and concentration to dryness under reduced pressure (2.7 kPa), the crystallized residue is stirred vigorously with isopropyl ether, drained, washed and recrystallized in cyclohexane (300 cc). The crystals are drained, washed with cyclohexane (2×15 cc) and dried to give (3aRS,7aRS)-2-benzyl-7,7-bis(3-fluorophenyl)perhydro-4-isoindolone (92 g) in the form of white crystals. M.p. 124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112988
Source datasetuspto-grants-1992_05
ORD IDord-378122067a414177ada82c0242fa5b17
Source noteuspto-grants-1992_05