HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531831Generated: November 3, 2026
1-Bromo-2-Chloroethane → HCID 21250993, compound
https://huagongshe.com/reaction/1531831
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-2-Chloroethane | HCID 7849 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-fluoro-N-(piperidin-4-yl)benzamide | HCID 4778226 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21250993 | HCID 21250993 | — |
Reaction Steps
A mixture of 4-(4-fluorobenzamido)piperidine (2 g; preparation 2), triethylamine (3.75 ml) and 1-bromo-2-chloroethane (1.11 ml) in 150 ml of dry tetrahydrofuran was refluxed overnight, then further triethylamine (3.75 ml) and 1-bromo-2-chloroethane (1.11 ml) were added. The mixture was refluxed for an additional 5 hours, treated again with 3.75 ml of triethylamine and 1.11 ml of 1-bromo-2-chloroethane and refluxed overnight. The reaction mixture was concentrated to a small volume, treated with ethyl acetate (200 ml) and the mixture washed with an aqueous saturated potassium carbonate solution. The organic phase was dried over sodium sulfate and concentrated to dryness. The residue (1.3 g) was crystallized from 10 ml of diethyl ether and dried under vacuum at 50° C., to give 1.06 g of the product, m.p. 220-225° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06200989B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-164a2a2e920f47b6b4f623242601d707 |
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| Source note | uspto-grants-2001_03 |
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