HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638192Generated: November 2, 2026
Hydrochloric Acid → HCID 13431749, compound
https://huagongshe.com/reaction/638192
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | 1-methyl-N-phenylpiperidin-4-amine | HCID 89642 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 13431749 | HCID 13431749 | 95% |
Reaction Steps
To a 2.03M solution of boron trichloride (20×1.2 mmol) in dichloroethane (11.8 ml) is dropwise added a solution of 4-anilino-1-methylpiperidine (3.81 g, 20 mmol) in dichloroethane (38 ml), and acetonitrile (2.1 ml, 20×1.2 mmol) is added to the mixture, which is heated under reflux over a period of 20 hours. After cooling, the reaction mixture is mixed with 2N hydrochloric acid (15 ml) and water (30 ml) and stirred at 100° C. over a period of 20 minutes. After cooling, the reaction mixture is mixed with conc. aqueous ammoniac solution and separated. The organic layer is washed with water, dried over anhydrous potassium carbonate and concentrated in vacuo to give 4-(2-acetylanilino)-1-methylpiperidine (4.41 g) as an oil. The yield is 95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04560684 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-beddad01415a4300a471ffd3d614ce74 |
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| Source note | uspto-grants-1985_12 |
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