HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384841Generated: October 29, 2026
Water → 1-(4-Fluoro-2-methoxyphenyl)piperazine
https://huagongshe.com/reaction/1384841
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Bis(2-chloroethyl)amine hydrochloride | HCID 522769 | — |
| Reactant | 4-Fluoro-2-methoxyaniline--hydrogen chloride (1/1) | HCID 21183846 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 1-(4-Fluoro-2-methoxyphenyl)piperazine | HCID 10488654 | 25% |
Reaction Steps
9 ml of chlorobenzene and H2O were distilled from a solution of 1.14 g of p-TosOH (6.03×10−3 moles) in 200 ml of chlorobenzene. The solution was cooled to 20° C. and then 1.19 g of 4-fluor-2-methoxyaniline hydrochloride (6.7×10−3 moles) and 1.31 g of bis (2-chloroethyl)amine hydrochloride (7.36×10−3 moles) were added. The reaction was held under reflux for 72 hours after which the solvent was removed and the residue was extracted with 5 ml of NaOH 2N and 30 ml of toluene. The organic phase was washed with H2O, was dried with Na2SO4 and the toluene was removed. The product was purified by silica column using dichloromethane/MeOH (9:1) as mobile phase. An oil was obtained. Yield: 25%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06262056B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-c557cffd5cd54ab384ce3a75a9b6c4f2 |
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| Source note | uspto-grants-2001_07 |
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