HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263081Generated: November 2, 2026
1-Chloro-2-(diethylamine)ethane hydrochloride → HCID 21318116, compound
https://huagongshe.com/reaction/263081
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloro-2-(diethylamine)ethane hydrochloride | HCID 13363 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(4-Chlorophenoxy)phenol | HCID 12346120 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21318116 | HCID 21318116 | 82.6% |
Reaction Steps
A solution of 13.2 g (0.075 mol) of 2-(N,N-diethylamino)-1-chloroethane hydrochloride in 30 ml of water is run over the course of 30 minutes into a solution, kept at about 60° C., of 15 g (0.068 mol) of p-(p-chlorophenoxy)-phenol and 6.3 g (0.157 mol) of sodium hydroxide pellets in 20 ml of water and 20 ml of ethanol. The mixture is heated to the reflux temperature for 1 hour and the ethanol is evaporated under reduced pressure. The aqueous phase is extracted with diethyl ether and the organic phase obtained is washed with water until neutral, dried over dry sodium sulphate and evaporated to dryness under reduced pressure. The oily residue is treated in a solution of hydrogen chloride in diethyl ether, to give 20 g of a white powder. Recrystallisation from ethyl acetate gives 18 g of CRL 40 330
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04156011 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-2fe8295884c74e5796c62d56892dcd3d |
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| Source note | uspto-grants-1979_05 |
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