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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(Diphenylmethylene)piperidine | HCID 2762533 | — |
| Reactant | 2-[2-(2-Chloroethoxy)ethoxy]-acetamide | HCID 20463153 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-[2-[2-[4-(Diphenylmethylene)-1-piperidinyl]ethoxy]ethoxy]-acetamide | HCID 20463151 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04443460 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-55c13fe774414739968eaee76683f1c2 |
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| Source note | uspto-grants-1984_04 |
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