HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189272Generated: October 30, 2026
Acetyl chloride → 1-[4-(4-Nitrophenyl)-1-piperidinyl]ethanone
https://huagongshe.com/reaction/2189272
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-(4-Nitrophenyl)piperidine | HCID 15925817 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[4-(4-Nitrophenyl)-1-piperidinyl]ethanone | HCID 58015948 | 110% |
Reaction Steps
To a solution of 4-(4-Nitro-phenyl)-piperidin (206 mg, 1 mmol) in CH2Cl2 (3 mL) is added AcCl (0.106 mL, 1.5 mmol) at 0° C. Then Et3N (0.253 mL, 1.8 mmol) is added slowly. The mixture is stirred at 0° C. for 10 minutes. Then saturated NaHCO3 aqueous solution is added. The aqueous layer is extracted with CH2Cl2, and the organic extracts are dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product is purified by column chromatography (SiO2, MeOH:CH2Cl2=0.7:99.3 to 6:93) to give 273 mg of the title compound as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324225B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-329d257e9d614ed5885aa7661ba30e77 |
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| Source note | uspto-grants-2012_12 |
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