HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248575Generated: October 31, 2026
Benzene → 2-[2-[4-(Diphenylmethyl)-1-piperazinyl]ethoxy]-acetamide
https://huagongshe.com/reaction/1248575
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Benzhydrylpiperazine | HCID 70048 | — |
| Reactant | 2-(2-Chloroethoxy)acetamide | HCID 11018931 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-[2-[4-(Diphenylmethyl)-1-piperazinyl]ethoxy]-acetamide | HCID 3068839 | 73% |
Reaction Steps
A mixture of 37.8 g (0.15 mole) of 1-(diphenylmethyl)-piperazine, 27.5 g (0.2 mole) of 2-(2-chloroethoxy)-acetamide and 26.5 g of anhydrous sodium carbonate in 120 ml of xylene is heated for 4 hours to 90° to 120° C. Thereafter, 120 ml of benzene are added to the reaction mixture, the precipitate formed is filtered off and the organic phase is extracted with dilute hydrochloric acid (30 ml of concentrated hydrochloric acid and 100 ml of water). 40 ml of a concentrated aqueous solution of sodium hydroxide are added, followed by extraction with benzene. The benzene solution is washed with water, dried over anhydrous sodium carbonate and the benzene is evaporated off to dryness. The evaporation residue is triturated with diethyl ether and left to crystallize. 2-[2-[4-(Diphenylmethyl)-1-piperazinyl]ethoxy]-acetamide is obtained in a yield of 73% of theory; M.P. 119°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04525358 |
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| Source dataset | uspto-grants-1985_06 |
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| ORD ID | ord-92ae43157e9a4f35b58fd2afe789a115 |
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| Source note | uspto-grants-1985_06 |
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