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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542786Generated: October 31, 2026

Ammonium Chloride → HCID 20207293, compound

https://huagongshe.com/reaction/542786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(3-Bromobenzyl)piperidineHCID 3847066—
ReactantMagnesiumHCID 5462224—
Reactant80236-09-5HCID 10630846—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20207293HCID 20207293—

Reaction Conditions

Temperature60 °C

Reaction Steps

10.2 g (0.04 mol) of 3-(1-piperidylmethyl)-bromobenzene in 20 ml of tetrahydrofuran are added dropwise to 0.97 g (0.04 mol) of magnesium filings in 5 ml of tetrahydrofuran at a reaction temperature of 60° C. This operation is followed by 30 minutes' stirring at 60° C., and the solution is then cooled to 10° C. 10.2 g (0.04 mol) of 2-benzylaminomethyl-oxirane in 20 ml of tetrahydrofurane are slowly added dropwise and the solution obtained is stirred at room temperature for 2 hours. After the addition of 20 ml of ice water and 4.5 g of ammonium chloride, the aqueous phase is separated and extracted with 25 ml of methylene chloride. The combined organic phases are dehydrated with sodium sulphate and concentrated by evaporation to yield a yellow resin which is chromatographed with methylene chloride/methanol (9:1) against silica gel. After concentration by evaporation, the second fraction yields the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659721
Source datasetuspto-grants-1987_04
ORD IDord-749847d6ca77459bb1360b14d8f5eee3
Source noteuspto-grants-1987_04