HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506847Generated: October 30, 2026
Dichloroacetic Acid → HCID 13076901, compound
https://huagongshe.com/reaction/1506847
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloroacetic Acid | HCID 6597 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | HCID 13076865 | HCID 13076865 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 13076901 | HCID 13076901 | — |
Reaction Steps
To a suspension of 1.6 g of NaH (60% dispersion in mineral oil) and 131 mg of 18-crown-6 ether in 60 ml of anhydrous dioxane, a solution of 16.4 ml of a solution of dichloroacetic acid (1 M) in anhydrous dioxane was slowly added at room temperature. The reaction mixture was heated to 60° C. and a solution of 3.2 g of 4-Chloro-2-(dicyclohexyl-hydroxy-methyl)-phenol in 42 ml anhydrous dioxane was added and stirred at 90° C. for 6 h. After cooling to 0° C., the reaction mixture was quenched with 8 ml of isopropanol and poured on ice. The aqueous phase was extracted with ether, then acidified with HCl (2 M, to pH 1), and extracted with ethyl acetate. The combined organic layers were dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was recrystallized from n-heptane to yield a bright yellow product. Yield: 2.5 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221784B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-e73b54e6d91949ccb8459958a571b2fb |
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| Source note | uspto-grants-2015_12 |
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