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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248927Generated: November 1, 2026

Hydrochloric Acid → HCID 12215669, compound

https://huagongshe.com/reaction/1248927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium MethoxideHCID 10942334—
ReactantAcetic acid, [(1-acetyl-2-methylpropyl)thio]-, methyl esterHCID 12215668—
SolventTolueneHCID 1140—
ProductHCID 12215669HCID 1221566987.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

204 g (1 mol) of 3-methoxycarbonylmethylthio-4-methyl-2-pentanone are added dropwise within one hour, at 0° C. with vigorous stirring, to a suspension of 108 g (2 mol) of freshly prepared sodium methylate in 2 liters of absolute toluene. The reaction mixture is stirred at 0° C. for a further 30 minutes, then poured into a mixture of 200 ml of concentrated hydrochloric acid and 800 ml of ice-water, and the organic phase is separated off, and the aqueous phase is extracted three times with dichloromethane. The combined organic phases are concentrated to 500 ml in vacuo and extracted with 500 ml of ice-cold 4N sodium hydroxide solution. The aqueous extracts are immediately acidified with a total of 400 ml of ice-cold hydrochloric acid and extracted three times with 200 ml of dichloromethane each time. The combined dichloromethane phases are dried over sodium sulphate and the solvent is removed in vacuo. The remaining solid is recrystallized from ligroin/ethanol. 150 g (87% of theory) of 2-isopropyltetrahydrothiopyran-3,5-dione of melting point 71° C. are obtained. ##STR53##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04628060
Source datasetuspto-grants-1986_12
ORD IDord-8687d1bae9474a8ea2f1f319dece9ce4
Source noteuspto-grants-1986_12