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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373021Generated: October 29, 2026

Hydrochloric Acid → HCID 14883922, compound

https://huagongshe.com/reaction/2373021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl acetoacetateHCID 7757—
ReactantSodium HydroxideHCID 14798—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 19902757HCID 19902757—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 14883922HCID 1488392289.6%

Reaction Steps

9.86 Grams of methyl acetoacetate were dissolved in 15 ml of water, and 12.67 g of a 30% aqueous sodium hydroxide solution was added thereto by drops while cooling the mixture to 25° C. or less. After having been stirred at 30°-35° C. for 3 hours, the mixture was adjusted to pH 7.0 with a concentrated aqueous hydrochloric acid solution. Thereafter, 0.74 g of potassium acetate and 2.42 g of tetrabutylammonium bromide were added thereto, and then an additional concentrated aqueous hydrochloric acid was added thereto so that the mixture had a pH of 6.9. Further, 28.00 g of a toluene solution containing 38.0% of 3-(3-methoxyphenylthio)butanal were added thereto and the resulting mixture was stirred at 45°-50° C. for 9 hours. The organic layer separated from the mixture was washed with a 5% aqueous acetic acid solution and then with a saturated aqueous sodium chloride solution. Then it was dried over anhydrous magnesium sulfate. Removing the solvent from the layer under reduced pressure gave 13.39 g of crude 4-hydroxy-6-(3-methoxyphenylthio)-2-heptanone (purity 90.9%, yield: 89.6%). A purified product was obtained by column chromatography. The purified product had an nD21 of 1.5530.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05101076
Source datasetuspto-grants-1992_03
ORD IDord-e8557507e3e442b888d8f331aaeac062
Source noteuspto-grants-1992_03