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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325889Generated: October 25, 2026

Benzene → 2-[2-[2-[4-(Diphenylmethylene)-1-piperidinyl]ethoxy]ethoxy]-acetamide

https://huagongshe.com/reaction/325889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantSodium CarbonateHCID 10340—
Reactant4-(Diphenylmethylene)piperidineHCID 2762533—
Reactant2-[2-(2-Chloroethoxy)ethoxy]-acetamideHCID 20463153—
SolventO-XyleneHCID 7237—
Product2-[2-[2-[4-(Diphenylmethylene)-1-piperidinyl]ethoxy]ethoxy]-acetamideHCID 2046315177%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 29.9 g of 4-(diphenylmethylene)-piperidine, 36.3 g of 2-[2-(2-chloroethoxy)ethoxy]-acetamide and 18 g of sodium carbonate in 80 ml of xylene is heated for 20 hours at a temperature of from 90°to 110° C. Thereafter, 80 ml of benzene are added thereto. The precipitate obtained is filtered off and the organic phase is extracted with a dilute solution of hydrochloric acid (20 ml of concentrated hydrochloride acid and 80 ml of water). After the addition of 30 ml of a concentrated solution of sodium hydroxide and extraction with benzene, the benzene solution obtained is washed, dried over anhydrous potassium carbonate and the benzene evaporated in vacuo. The 2-[2-[2-[4-(diphenylmethylene)-1-piperidinyl]ethoxy]ethoxy]-acetamide obtained is used as such for the preparation of the corresponding acid (see Example 3.4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04443460
Source datasetuspto-grants-1984_04
ORD IDord-55c13fe774414739968eaee76683f1c2
Source noteuspto-grants-1984_04