HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234817Generated: October 26, 2026
Water → 4-[4-(3,3-Dichloroprop-2-enyloxy)-2,6-dichlorophenoxy]butyl acetate
https://huagongshe.com/reaction/2234817
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,1,1,3-Tetrachloropropane | HCID 14056 | — |
| Reactant | 4-(2,6-Dichloro-4-hydroxyphenoxy)butyl acetate | HCID 57838141 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[4-(3,3-Dichloroprop-2-enyloxy)-2,6-dichlorophenoxy]butyl acetate | HCID 18429500 | 78.4% |
Reaction Steps
A solution of 25.3 grams (0.086 mole) of 4-(2,6-dichloro-4-hydroxyphenoxy)butyl acetate in 250 mL of DMF was stirred, and 19.5 grams (0.1 mole) of 1,1,1,3-tetrachloropropane was added, followed by 18 grams (0.13 mole) of potassium carbonate. Upon completion of addition the reaction mixture was heated at 80° C. during a 17 hour period. After this time the reaction mixture was cooled to ambient temperature, stirred with 350 mL of water and extracted with four 150 mL portions of diethyl ether. The combined extracts were washed with two 100 mL portions of water, dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residue. The residue was purified with column chromatography on silica gel using 1:1 methylene chloride:hexane as an eluant. The appropriate fractions were combined and concentrated under reduced pressure, yielding 27.1 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713970B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-62c566b93eea487293e5af09845f56a3 |
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| Source note | uspto-grants-2010_05 |
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