Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444503Generated: October 27, 2026

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

https://huagongshe.com/reaction/1444503

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 into 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. According to the conventional 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 numberUS07662821B2
Source datasetuspto-grants-2010_02
ORD IDord-a33eac40f72b4902a9c049ac7795824d
Source noteuspto-grants-2010_02