HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620602Generated: November 5, 2026
Water → 1-[2,4-Bis(trifluoromethyl)benzyl]-2-oxopiperidine-4-carboxylic acid
https://huagongshe.com/reaction/1620602
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,4-Bis(trifluoromethyl)benzyl bromide | HCID 518871 | — |
| Reactant | 2-Oxopiperidine-4-carboxylic acid | HCID 55286080 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[2,4-Bis(trifluoromethyl)benzyl]-2-oxopiperidine-4-carboxylic acid | HCID 86678773 | 58.2% |
Reaction Steps
To a solution of 2-oxopiperidine-4-carboxylic acid (21.3 g) in tetrahydrofuran (300 mL) was added 60% sodium hydride (18 g, containing mineral oil) under cooling to 0° C. The reaction mixture was stirred for 30 min under cooling to 0° C. To the reaction mixture was added dropwise 1-(bromomethyl)-2,4-bis(trifluoromethyl)benzene (46 g) under cooling to 0° C., and the mixture was further stirred at 80° C. for 2 days. Water was added to the reaction mixture under cooling to 0° C., and the mixture was extracted with ethyl acetate. To the aqueous layer was further added 10% hydrochloric acid, and the mixture was extracted with ethyl acetate. The extract was dried over sodium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (32 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772277B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-6f0cb7cf409f4b6da26145a8fe848f96 |
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| Source note | uspto-grants-2014_07 |
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