HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978349Generated: October 29, 2026
Water → N-(3-phenylpropan-1-yl)-N-[1-tert-butoxycarbonylpiperidin-4-ylmethyl]trifluoroacetamide
https://huagongshe.com/reaction/1978349
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | (3-Bromopropyl)benzene | HCID 12503 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(1-tert-butoxycarbonylpiperidin-4-ylmethyl)trifluoroacetamide | HCID 21994020 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(3-phenylpropan-1-yl)-N-[1-tert-butoxycarbonylpiperidin-4-ylmethyl]trifluoroacetamide | HCID 21993736 | — |
Reaction Steps
Under nitrogen, 0.25 g (6.25 mM) of a 60% suspension of sodium hydride in liquid paraffin was added to a solution of 1.73 g (5.57 mM) of N-(1-tert-butoxycarbonylpiperidin-4-ylmethyl)trifluoroacetoamide in N,N-dimethylformamide (20 ml) at 0° C. and the mixture was stirred at 0° C. for 30 minutes. To this mixture was added 1.0 ml (6.58 mM) of 1-bromo-3-phenylpropane and the mixture was stirred at room temperature for 2.5 hours and further at 60° C. for one hour. The reaction was stopped by adding water and the reaction mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium chloride, dried over MgSO4, and purified by column chromatography (ethyl acetate-hexane 30%) to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06235731B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-cf9322ae1a1a46739cfa3037d28cc2f0 |
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| Source note | uspto-grants-2001_05 |
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