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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075851Generated: November 3, 2026

Nanofin → HCID 21541283, compound

https://huagongshe.com/reaction/1075851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNanofinHCID 68843—
ReactantHCID 21541295HCID 21541295—
SolventEthanolHCID 702—
ProductHCID 21541283HCID 2154128374.3%

Reaction Steps

A mixture of 5.2 g of 1-chloro-3-[2-(2-methoxyethoxy)phenoxy]-2-propanol, 4.6 g of 2,6-dimethylpiperidine and 50 ml of ethanol is refluxed for 16 hours. The ethanol is removed, and ether is added to the residue. The insoluble matter is filtered off, and the filtrate is extracted with two 80 ml portions of 10% hydrochloric acid. The aqueous layer is made alkaline with sodium hydroxide, and the separated oil is extracted twice with ether. The ether layer is dried over anhydrous potassium carbonate, and the ether is removed to give 5.0 g of 1-(2,6-dimethylpiperidino)-3-[2-(2-methoxyethoxy)phenoxy]-2-propanol, melting at 92°-94°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954776
Source datasetuspto-grants-1976_05
ORD IDord-cf7bb7ec85a8473d88625faa010d4063
Source noteuspto-grants-1976_05