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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443235Generated: October 27, 2026

Hydrochloric Acid → Ethyl-4-(3-isopropyl-2-methoxyphenyl)-4-methyl-2-oxo-pentanoate

https://huagongshe.com/reaction/1443235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
ReactantTin tetrachlorideHCID 24287—
Reactant2-Trimethylsilanyloxy-acrylic acid ethyl esterHCID 11116806—
Reactant2-(3-Isopropyl-2-methoxyphenyl)propan-2-olHCID 17989199—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductEthyl-4-(3-isopropyl-2-methoxyphenyl)-4-methyl-2-oxo-pentanoateHCID 1798913249.3%

Reaction Conditions

Temperature-72 °C

Reaction Steps

15.3 ml (129.71 mmol) of tin tetrachloride is added in drops to a mixture, cooled to −72° C., that consists of 28.16 g (135.19 mmol) of 2-(3-isopropyl-2-methoxyphenyl)-propan-2-ol and 50.9 g (270.38 mmol) of 2-trimethylsilanyloxy-acrylic acid ethyl ester in 420 ml of dichloromethane. In this case, the temperature increased to −65° C. After 30 minutes of stirring in this temperature interval, the reaction mixture is poured onto a mixture that consists of saturated sodium carbonate solution and dichloromethane (in each case 250 ml). After 30 minutes of stirring at room temperature, the batch is transferred into a spherical separating funnel, and a 1:1 mixture that consists of water and dichloromethane is added until a phase separation takes place. After the organic phase is shaken with sodium carbonate, 1N HCl and water, it is dried with sodium sulfate. After the usual procedure, the residue is chromatographed on silica gel (mobile solvent: ethyl acetate/hexane). 20.44 g (48.35%) of the desired compound is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659297B2
Source datasetuspto-grants-2010_02
ORD IDord-ef13a7846ab1487e8c46e74cbb13d7ca
Source noteuspto-grants-2010_02