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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278293Generated: October 30, 2026

Dichloroacetic Acid → HCID 53645250, compound

https://huagongshe.com/reaction/1278293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloroacetic AcidHCID 6597—
ReactantSodium hydrideHCID 24758—
ReactantHCID 13076850HCID 13076850—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 53645250HCID 5364525075.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 14.18 g of dichloroacetic acid in 150 ml of dioxane was added with stirring at room temperature to a mixture of 11.8 g of sodium hydride as a 50% oil suspension, 120 ml of dioxane and 1.05 g of dibenzo-18-courone-6 and then a solution of 20.74 g of the product of Step B in 250 ml of dioxane was added dropwise thereto. The mixture was stirred at 80° C. for 2 hours and was cooled and poured into ice. The aqueous phase was washed with 300 ml of ether, was acidified with 30 ml of concentrated hydrochloric acid and was extracted 3 times with 250 ml of ether. The ether phase was washed twice with 100 ml of water and was extracted twice with 250 ml of aqueous 5% sodium bicarbonate solution. The aqueous phase was washed with 100 ml of ether, acidified with 60 ml of concentrated hydrochloric acid and was extracted 3 times with 250 ml of ether. The decanted organic phase was washed with water until the wash water was neutral, dried over magnesium sulfate and was evaporated to dryness under reduced pressure to obtain 18.7 g of raw 6-cyclohexyl-4-methyl-4-phenyl-[4H]-1,3-benzodioxin-2-carboxylic acid (mixture of 2 diastereoisomeric racemates).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04281012
Source datasetuspto-grants-1981_07
ORD IDord-6773ed65e0a34d069cbf9daab6a4bd8f
Source noteuspto-grants-1981_07