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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417809Generated: October 25, 2026

1-Formyl-4-(2-bromo-4-methoxyphenyl)piperazine → 1-(2-Bromo-4-methoxyphenyl)piperazine

https://huagongshe.com/reaction/1417809

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Formyl-4-(2-bromo-4-methoxyphenyl)piperazineHCID 23288818—
SolventHydrochloric AcidHCID 313—
Product1-(2-Bromo-4-methoxyphenyl)piperazineHCID 23288928—

Reaction Steps

A mixture of 1-formyl-4-(2-bromo-4-methoxyphenyl)piperazine (VII, 3.92 g, 3.1 mmol) and hydrochloric acid (4N, 70 ml) is heated at 100° for 50 min. The mixture is then concentrated under reduced pressure to remove most of the aqueous hydrochloric acid. Saturated sodium bicarbonate is then cautiously added and the aqueous phase is extracted with dichloromethane. The combined organic phase is backwashed with saline, dried over magnesium sulfate, and concentrated to give 1-(2-bromo-4-methoxyphenyl)piperazine (VIII), NMR (CDCl3) 2.55, 2.95, 3.08, 3.77, 6.83, 7.01, 7.14 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877317
Source datasetuspto-grants-1999_03
ORD IDord-adba3b0f6a4f4aa382e2cf38ed387201
Source noteuspto-grants-1999_03