HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936566Generated: November 4, 2026
p-Bromobenzenesulfonyl chloride → HCID 1219636, compound
https://huagongshe.com/reaction/1936566
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 1219636 | HCID 1219636 | 100.1% |
Reaction Steps
A solution of 4-bromophenyl sulphonyl chloride (53.76 g) in dichloromethane (700 ml) was added to a stirred solution of ethyl piperidine-4-carboxylate (32.97 g) in dichloromethane (500 ml) containing triethylamine (36 ml) at 0° C. and under argon over 0.75 hours. The reaction was stirred for 18 hours. The reaction mixture was washed with water (2×500 ml), saturated brine (1×500 ml), dried and evaporated. The residual solid was triturated in isohexane (500 ml) for 1 hour, collected by filtration and dried to give, as a colourless solid, ethyl 1-(4-bromophenylsulphonyl)piperidine-4-carboxylate (79 g); mp 132-3° C.; NMR (CDCl3): 1.21(t, 3H), 1.70-1.90(m, 2H), 1.90-2.05(m, 2H), 2.18-2.33(m, 1H), 2.45-2.60(m, 2H), 3.53-3.67(m, 2H), 4.10(q, 2H), 7.55-7.70(m, 4H); EI-MS m/z 376 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06391880B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-cb45392aa6b64c2eb4a9cc8857d1fb2b |
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| Source note | uspto-grants-2002_05 |
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