HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416294Generated: October 27, 2026
Potassium Carbonate → 1-(3-Chloro-4-methoxyphenyl)piperazine
https://huagongshe.com/reaction/1416294
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-4-methoxyaniline | HCID 407432 | — |
| Reactant | Bis(2-chloroethyl)amine hydrochloride | HCID 522769 | — |
| Reactant | Sodium bicarbonate water | HCID 86585896 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 1-(3-Chloro-4-methoxyphenyl)piperazine | HCID 4739562 | 32.6% |
Reaction Steps
A mixture of 3-chloro-4-anisidine (Aldrich; 0.633 g), bis(2-chloroethyl)amine hydrochloride (Aldrich; 0.860 g), potassium carbonate (1.11 g), and N,N-dimethylacetamide (6 mL) is stirred at 100° C. for 17.5 h, at which time the mixture is cooled and partioned between dichloromethane and water/sodium bicarbonate. The organic layers are dried over sodium sulfate, concentrated, and the residue is chromatographed on silica gel using methanol/dichloromethane (8/92) to give 0.297 g of 1-(3-chloro-4-methoxyphenyl)piperazine. 1H NMR (CDCl3) δ3.05, 3.86, 6.80, 6.87, 6.99.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05912246 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-e66c4b046a254884acf15bca64dc9962 |
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| Source note | uspto-grants-1999_06 |
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