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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893285Generated: October 29, 2026

Hydrochloric Acid → HCID 18955939, compound

https://huagongshe.com/reaction/893285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant1-[(3-Bromophenyl)(4-chlorophenyl)methyl]-4-methylpiperazineHCID 18955927—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 18955939HCID 18955939—

Reaction Conditions

Temperature-78 °C

Reaction Steps

1-(3-Bromo-4'-chlorobenzhydryl)-4-methylpiperazine (see U.S. Pat. No. 4,757,074) (1.00 g, 2.63 mmole) was dissolved in 12 ml of dry tetrahydrofuran under nitrogen and cooled to -78° C. A solution of 1.1 M n-butyllithium in hexane (2.4 ml) was added dropwise and the reaction was stirred for ten minutes. N,N-Dimethylformamide (0.25 ml, 3.2 mmole) was added in one portion and the reaction was allowed to warm to -40° C. Hydrochloric acid (1.0 M, 20 ml) was added and the reaction was warmed to room temperature. The solution was washed with 20 ml of diethyl ether and the ethereal wash was discarded. The aqueous solution was made basic with aqueous sodium hydroxide and extracted with two 15 ml portions of chloroform. The combined chloroform extracts were dried over sodium sulfate and the solvent removed to give 738 mg of crude 1-(4-chloro-3'-formylbenzhydryl)-4-methylpiperazine as a dark oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05124330
Source datasetuspto-grants-1992_06
ORD IDord-e1b2c893f6a1498a8c01b164bea0770a
Source noteuspto-grants-1992_06