HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180075Generated: November 1, 2026
Diphosgene → 4-Phenyl-piperidine-1-carboxylic acid 4-(5-methyl-pyridin-2-ylmethyl)-phenyl ester
https://huagongshe.com/reaction/1180075
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | 4-Phenylpiperidine | HCID 69873 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(5-Methyl-pyridin-2-ylmethyl)phenol | HCID 22047848 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Phenyl-piperidine-1-carboxylic acid 4-(5-methyl-pyridin-2-ylmethyl)-phenyl ester | HCID 69517969 | 28% |
Reaction Steps
To a solution of 4-(5-methyl-pyridin-2-ylmethyl)phenol (0.8 mmol) prepared as described above and ethyldiisopropylamine (1.5 mmol) in CH2Cl2 (5 mL) at −30° C. was added trichloromethyl chloroformate (1.0 mmol). The solution was stirred at −30° C. for 10 min and at reflux temperature for 2 h. The solution was evaporated to dryness and redissolved in CH2Cl2 (5 mL) and cooled to 0° C. before addition of 4-phenylpiperidine (1.5 mmol). The solution was stirred at room temperature for 16 h evaporated to give the crude product which was purified by FC (Quad flash 40 CH2Cl2:Et2O:Heptane:Et3N 1:1:2:0.25->1:1:1:0.25) to give the title compound in 28% yield as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07279470B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-cfb4e9480a7c4414861481fc4c3c9059 |
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| Source note | uspto-grants-2007_10 |
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