Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098965Generated: October 31, 2026

Methyl (trimethylsilyl)acetate → (E)-Methyl 2-(6-(benzyloxy)-2,2-dimethyl-2,3-dihydroinden-1-ylidene)acetate

https://huagongshe.com/reaction/2098965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl (trimethylsilyl)acetateHCID 76210—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant6-(Benzyloxy)-2,2-dimethyl-2,3-dihydroinden-1-oneHCID 59590882—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(E)-Methyl 2-(6-(benzyloxy)-2,2-dimethyl-2,3-dihydroinden-1-ylidene)acetateHCID 5959093845%

Reaction Conditions

Temperature-78 °C

Reaction Steps

At −78° C., lithium bis(trimethylsilyl)amide (1.0 M in THF) (3.6 mL, 3.6 mmol) was added slowly to a solution of methyl 2-(trimethylsilyl)acetate (0.59 mL, 3.6 mmol) in THF (20 mL). The mixture was maintained at −78° C. for 7 minutes and then 6-(benzyloxy)-2,2-dimethyl-2,3-dihydroinden-1-one (8.3) (0.535 g, 2.0 mmol) was added in one portion. The resulting mixture was stirred at −78° C. and allowed to warm to room temperature overnight. The reaction mixture was then diluted with EtOAc (200 mL), washed with water and brine, and dried over anhydrous sodium sulfate. After removing solvent, the residue was purified by chromatography (silica gel, 1:5 EtOAc/hexane) to give product 8.4 in 45% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450522B2
Source datasetuspto-grants-2013_05
ORD IDord-49a907eaa4cc4f1ea9d5b4248f92bb8d
Source noteuspto-grants-2013_05