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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 41693Erstellt: 24. Oktober 2026

Triethylamine → Benzyl 4-(4-bromophenyl)piperazine-1-carboxylate

https://huagongshe.com/de/reaction/41693

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktBenzyl chloroformateHCID 10387—
Edukt1-(4-Bromophenyl)piperazineHCID 2735629—
LösungsmittelDichloromethaneHCID 6344—
ProduktBenzyl 4-(4-bromophenyl)piperazine-1-carboxylateHCID 46739494—

Reaktionsschritte

5 g of 4-bromophenylpiperazine are placed in a 500 ml three-necked flask under a nitrogen atmosphere. 4.34 ml of triethylamine are added. The mixture is cooled in an ice bath and 3.24 ml of benzyl chloroformate are added. The mixture is allowed to return to ambient temperature. It is diluted with dichloromethane and then gentle hydrolysis is carried out. The aqueous phase is extracted with dichloromethane. The organic phases are combined, washed with a saturated NaCl solution, dried over sodium sulphate, then filtered through a sintered glass filter and concentrated under vacuum. 8.43 g of 4-(4-bromophenyl)piperazine-1-carboxylic acid benzyl ester are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530657B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-c53fbf5f16654f649222fece5a7bfb47
Quellennotizuspto-grants-2013_09