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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484130Generated: October 28, 2026

1-(2-Methoxyphenyl)piperazine → HCID 14856167, compound

https://huagongshe.com/reaction/484130

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 21706595HCID 21706595—
CatalystSodium IodideHCID 5238—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 14856167HCID 1485616799.7%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 3-(4-bromobutyl)-1,4-dioxothiazolidine (3.37 g), 1-(2-methoxyphenyl)piperazine (2.80 g), K2CO3 (4.60 g), NaI (190 mg) and CH3CN (150 ml) was heated at reflux (bath temperature 95° C.) for 24 h. TLC analysis (silica gel, 20% MeOH/CH2Cl2) showed the consumption of the starting sulfoxide and the presence of one major product with Rf =0.43. The mixture was cooled to room temperature, EtOAc (100 m) was added and the mixture was filtered. The filtrate was concentrated in vacuo to an oil which was filtered through silica gel using 20% MeOH/CH2Cl2 as the eluent. The fractions containing the material with Rf =0.43 were concentrated in vacuo to yield 4.83 g of a foam, which was dissolved in MeOH/CH2Cl2 and flash chromatographed (silica gel) to yield 3.28 g of a crude product. Rechromatography over silica gel using 50% MeOH/toluene as eluent yielded 2.98 g of an oil which solidified on standing. The solid was dissolved in 50% MeOH/EtOAc and filtered through silica gel. The filtrate containing the product was concentrated to approximately 5 ml and the oily liquid was seeded and left standing, yielding 0.91 g of a white solid, mp, 111°-113° C. The mother liquor was concentrated in vacuo to a solid which was recrystallized from CH2Cl2 /Et2O, yielding an additional 0.79 g of fine needles, mp, 111°-113° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05229388
Source datasetuspto-grants-1993_07
ORD IDord-85030be79fae45a691af000496c1651d
Source noteuspto-grants-1993_07