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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441984Generated: October 31, 2026

1-Piperazinecarboxylic acid, ethyl ester → HCID 21416190, compound

https://huagongshe.com/reaction/441984

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Piperazinecarboxylic acid, ethyl esterHCID 8431—
ReactantHCID 12232370HCID 12232370—
SolventChloroformHCID 6212—
ProductHCID 21416190HCID 21416190—

Reaction Steps

24 G. of 2,10-dichloro-8-fluoro-10,11-dihydro-dibenzo[b,f]thiepin in 80 ml. of chloroform are heated together with 38.4 g. of 1-carbethoxy-piperazine under reflux conditions for 20 hours. The reaction mixture is poured over ice water and extracted with chloforom. The organic phase is dried over magnesium sulfate and evaporated under reduced pressure, whereby there is obtained oily 1-carbethoxy-4-(2-chloro-8-fluoro-10,11-dihydro-dibenzo [b,f]thiepin-10-yl)-piperazine. 24.5 G. of 1-carbethoxy-4-(2-chloro-8-fluoro-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-piperazine, 350 ml. of ethyleneglycol, 19 g. of potassium hydroxide and 1.5 ml. of water are heated together at 160° for 1 hours. The reaction mixture is poured over water and extracted with chloroform. The organic phase is washed with water, dried over magneisum sulfate and evaporated under reduced pressure, whereby there is obtained 1-(2-chloro-8-fluoro-10,11-dihydro-dibenzo[b,f]-thiepin-10-yl)-piperazine as a thick oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04044010
Source datasetuspto-grants-1977_08
ORD IDord-25a8b4f56c634c33a6daec6958697d37
Source noteuspto-grants-1977_08