HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019262Generated: October 31, 2026
Benzenesulfonyl chloride → HCID 5314675, compound
https://huagongshe.com/reaction/1019262
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Piperonylamine | HCID 2723901 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 5314675 | HCID 5314675 | 83.2% |
Reaction Steps
To a solution of 4-piperidone monohydrate hydrochloride (4.59 g, 30 mmol), triethylamine (12.5 ml, 90 mmol) in CH2Cl2 (50 ml) was added benzenesulfonyl chloride (5.30 g, 30 mmol). The mixture was stirred at 25° C. for 16 h. After evaporation of solvents, the residue was triturated with water (100 ml), filtered, and further purified by recrystallization from hexanes/CH2Cl2 (3:1) to afford the desired ketone (5.97 g, 83%) as a colorless solid. mp 116-118° C.; 1H NMR (500 MHz, CDCl3) δ2.54 (t, J=6.4Hz, 4H), 3.41(t, J=6.4Hz, 4H), 7.58 (d, J =7.8 Hz, 2H), 7.63 (t, J=7.0 Hz, 1H), 7.81 (d, J=7.8 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06486199B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-8a7b44dbc01f4e71822a8133f3f8f721 |
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| Source note | uspto-grants-2002_11 |
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