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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974635Generated: October 29, 2026

1-Phenylpiperazine → HCID 15053397, compound

https://huagongshe.com/reaction/974635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Chlorocarbonyl-3-[3-(trifluoromethyl)phenoxy]azetidineHCID 19799606—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15053397HCID 1505339754.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A mixture of 2.8 g (0.01 mole) of 3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarbonyl chloride and 1.4 g (0.01 mole) of potassium carbonate in 25 ml of tetrahydrofuran was stirred for 10 min then 1.6 g (0.01 mole) of 1-phenylpiperazine was added. After stirring for 30 min, approximately 2 g of ice was added and stirring continued for 18 hr. The reaction mixture was diluted with 200 ml of water and the oil which separated was extracted into methylene chloride (2×50 ml), dried and concentrated in vacuo to yield 5.1 g of crude dark yellow oil, which solidified when cooled to -78° C. Recrystallization from isopropyl ether yielded 2.2 g (54.3%) of pale yellow crystals, m.p. 93°-94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05068231
Source datasetuspto-grants-1991_11
ORD IDord-d54858038ecb4f1f80b82662d27e1b16
Source noteuspto-grants-1991_11