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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190262Generated: October 26, 2026

Acetic Acid → 1-(4-Bromophenyl)-4-methylpiperazine

https://huagongshe.com/reaction/2190262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactant1-(4-Bromophenyl)piperazine hydrochlorideHCID 14422838—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product1-(4-Bromophenyl)-4-methylpiperazineHCID 1181767597.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-(4-bromophenyl)piperazine hydrochloride (1.0 g, 3.61 mmol), formaldehyde (37% aqueous, 3 mL, 39.71 mmol), AcOH (0.23 mL, 3.97 mmol) and MeOH (30 mL) was heated at 80° C. under nitrogen. After 1.5 hours, the mixture was cooled to 0° C. in an ice bath. Methylene chloride (5 mL) was added followed by a slow addition of sodium borohydride (1.91 g, 50.54 mmol) under nitrogen. The mixture was stirred for 1 hour and then poured into a seperatory funnel containing a saturated solution of NH4Cl (25 mL) and CH2Cl2 (50 mL). The layers were separated and the aqueous layer was extracted with CH2Cl2 (2×50 mL). The extracts were dried (Na2SO4), filtered and concentrated to to give the sub-title compound (900 mg, 97%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324264B1
Source datasetuspto-grants-2012_12
ORD IDord-25faed18ce264f8ea9d8e6eb50cfa2ac
Source noteuspto-grants-2012_12