Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394921Generated: October 29, 2026

Hydrochloric Acid → HCID 69682206, compound

https://huagongshe.com/reaction/394921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylsilaneHCID 12052—
ReactantTrimethylsilyl triflateHCID 65367—
ReactantButoxytrimethylsilaneHCID 519537—
ReactantHCID 21267561HCID 21267561—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 69682206HCID 6968220656.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

6 g of oxo-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-acetic acid ethyl ester and 2.6 g of butoxytrimethylsilane were dissolved in 200 ml of methylene chloride. The solution was cooled to 0° C., treated with 400 mg of trimethylsilyl triflate and stirred at 0° C. for 1.5 hours. After the dropwise addition of 2 g of triethylsilane, the reaction mixture was stirred at room temperature for 26 hours, then diluted with 500 ml of water, acidified with 2N hydrochloric acid and extracted with ether. The organic phase was washed with water, dried (Na2SO4) and the solvent evaporated. The oily residue was purified with flash chromatography (silica gel, eluent hexane/tert.butyl methyl ether 3%) and preparative HPLC (YMC CN 60 Å5-15 μm, hexane) to give 3.5 g of the title product as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06603012B2
Source datasetuspto-grants-2003_08
ORD IDord-eefd3b6428104b38931fccb5974de1ea
Source noteuspto-grants-2003_08