HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325592Generated: October 25, 2026
Triethylamine → 2-(2,6-Dichlorobenzyloxy)ethyl 2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate
https://huagongshe.com/reaction/325592
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-{4-[4-(Trifluoromethyl)phenoxy]phenoxy}propanoyl chloride | HCID 12906015 | — |
| Reactant | Ethanol, 2-((2,6-dichlorophenyl)methoxy)- | HCID 13341669 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(2,6-Dichlorobenzyloxy)ethyl 2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate | HCID 13341670 | 93% |
Reaction Steps
22.1 g of 2-(2,6-dichlorobenzyloxy)ethanol and 10.1 g of triethylamine were dissolved in 200 ml of toluene, then cooled to 0° C. To this solution was dropwise added a solution of 34.5 g of 2-[4-(4-trifluoromethylphenoxy)phenoxy]propionyl chloride in 50 ml of toluene at 0° to 10° C. After the dropwise addition, the reaction mixture was gradually heated and, at 40° C., it was stirred for one hour to complete the reaction. After cooling the reaction solution to room temperature, it was washed successively with 1% strength by weight sodium hydroxide aqueous solution and water, then dehydrated. After distilling off toluene under reduced pressure, the resulting colorless, viscous, oily product was allowed to stand for about 1 month to obtain 49.2 g of crystalline 2-(2,6-dichlorobenzyloxy)ethyl 2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate. m.p. 51° to 53° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04441913 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-81c65e9b7c0842f0b1004984e7e6694b |
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| Source note | uspto-grants-1984_04 |
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