HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196237Generated: October 31, 2026
Trifluoroacetic acid → HCID 67915874, compound
https://huagongshe.com/reaction/1196237
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-Benzyl-1-butoxy-N-[(trimethylsilyl)methyl]methanamine | HCID 11097910 | — |
| Reactant | 4,4-Bis(3-fluorophenyl)cyclohexenone | HCID 54307328 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67915874 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05112988 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-378122067a414177ada82c0242fa5b17 |
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| Source note | uspto-grants-1992_05 |
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