HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091744Generated: October 31, 2026
Triethylamine → 3-Methyl 1-(4-nitrophenyl) 5-[4-(trifluoromethyl)phenyl]piperidine-1,3-dicarboxylate
https://huagongshe.com/reaction/2091744
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | Methyl 5-(4-(trifluoromethyl)phenyl)piperidine-3-carboxylate | HCID 58002265 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Methyl 1-(4-nitrophenyl) 5-[4-(trifluoromethyl)phenyl]piperidine-1,3-dicarboxylate | HCID 58002325 | — |
Reaction Steps
20.0 g (69.6 mmol) of methyl 5-[4-(trifluoromethyl)phenyl]piperidine-3-carboxylate (Example 13A) were dissolved in 1.0 l of dichloromethane, and admixed at 0° C. with 14.1 g (139 mmol) of triethylamine Subsequently, 14.0 g (69.6 mmol) of 4-nitrophenyl chlorocarbonate were added dropwise. The reaction mixture was stirred at 0° C. for 2 h and then at RT for 16 h. For workup, the mixture was washed with saturated aqueous sodium hydrogencarbonate solution. The organic phase was dried over magnesium sulphate, filtered and concentrated under reduced pressure. This gave 31.3 g of crude product, which was reacted without any further purification steps.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440657B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-df2483d00bfc43e08c14826da530e556 |
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| Source note | uspto-grants-2013_05 |
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