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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848515Generated: October 30, 2026

Hydrochloric Acid → HCID 20565503, compound

https://huagongshe.com/reaction/848515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Chloro-2-nitrobenzeneHCID 6945—
ReactantSodium hydrideHCID 24758—
Reactant3-(Dimethylamino)-1-phenylpropan-1-olHCID 110665—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 20565503HCID 2056550376%

Reaction Conditions

Temperature25 °C

Reaction Steps

70 ml of dimethylsulfoxide were added over 10 minutes at 60°-65° C. to a mixture of 20 ml of dimethylsulfoxide and 9.2 g of sodium hydride in a 50% oil disperson and after cooling the mixture to 25° C., 17.28 g of N,N-dimethyl-3-phenyl-3-hydroxy-propanamine were added thereto. The temperature returned to room temperature and 25.2 g of o-chloro-nitrobenzene were added thereto. The mixture was held at 25° C. for one hour and was then extracted with ethyl acetate. The organic phase was washed with water, dried and evaporated to dryness to obtain 41 g of raw product which was taken up twice in 100 ml of N hydrochloric acid. The neutral fraction was extracted twice with 400 ml of ether and the aqueous phase was made alkaline by addition of 50 ml of sodium hydroxide solution. The mixture was extracted with methylene chloride and the organic phase was washed with water, dried and treated with activated carbon. The mixture was filtered and the filtrate was evaporated to dryness to obtain 22 g of N,N-dimethyl-γ-(2-nitrophenoxy)-benzene-propanamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04296126
Source datasetuspto-grants-1981_10
ORD IDord-282e1eebafaa46d08d59a6ec9a87a87e
Source noteuspto-grants-1981_10