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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724002Generated: November 2, 2026

Chlorotrimethylsilane → HCID 68649276, compound

https://huagongshe.com/reaction/1724002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDiisopropylamineHCID 7912—
ReactantHCID 9799516HCID 9799516—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68649276HCID 6864927674%

Reaction Conditions

Temperature-78 °C

Reaction Steps

i-Pr2NH (0.556 mL, 4.04 mmol), distilled from CaH, was added to THF (7 mL) and cooled to −78° C. A solution of n-BuLi (2.59 M in THF, 1.56 mL, 4.04 mmol) was added dropwise. After completion of addition the reaction mixture stirred at −30° C. for 35 minutes and then cooled down again to −78° C. TMS-Cl (0.546 mL) and 1-(2,2-dimethyl-chroman-6-yl)-2-(3,4,5-trimethoxy-phenyl)-ethanone (1.20 g, 3.23 mmol) dissolved in THF (25 mL) were added dropwise to the stirring reaction mixture. After completion of addition the reaction mixture continued stirring at −78° C. for an additional 30 minutes before being warmed up to −30° C. After stirring at −30° C. for 1 hour the reaction was diluted with diethyl ether and warmed to room temperature. At room temperature the reaction mixture was concentrated and the resulting crude material was purified using silica gel chromatography (4:1 pentane: ethyl acetate to 1:1 pentane: ethyl acetate) to obtain the desired compound (879.1 mg, 74% yield based on recovered starting material).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485283B2
Source datasetuspto-grants-2009_02
ORD IDord-060715dd5e044a1390315db3a213d6e3
Source noteuspto-grants-2009_02