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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867679Generated: October 25, 2026

Phenethyl bromide → 1-(2-Phenylethyl)-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromide

https://huagongshe.com/reaction/867679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantSodium hydrideHCID 24758—
ReactantEther hydrobromideHCID 86739792—
ReactantHCID 178480237HCID 178480237—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product1-(2-Phenylethyl)-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromideHCID 1403251136%

Reaction Steps

To a stirred mixture of 0.86 g of sodium hydride (50% oil dispersion) in 50 ml of dimethylformamide was added, dropwise, 3.0 g of 3-(1-methyl-4-piperidinyl)-1H-indazole in 15 ml of hot dimethylformamide. The reaction mixture was stirred at ambient temperature for 1 hr and then a solution of 3.33 g of (2-bromoethyl)benzene in 10 ml of dimethylformamide was added dropwise. The reaction mixture was stirred for 21/2 days at ambient temperature, cooled to 0°, and water was added dropwise. The mixture was extracted with ethyl acetate, washed with water, dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to yield an oil. The oil was dissolved in ether and a saturated hydrogen bromide/ether solution was added dropwise. The resultant solid was recrystallized two times from ethanol to yield 2.0 g (36%) of product, mp 163°-164° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775761
Source datasetuspto-grants-1988_10
ORD IDord-c9c8ee696491410f8e34cf17c0f09e12
Source noteuspto-grants-1988_10