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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604350Generated: November 2, 2026

Chlorotrimethylsilane → HCID 13227592, compound

https://huagongshe.com/reaction/1604350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDiisopropylamineHCID 7912—
ReactantEthyl cyclopropaneacetateHCID 12453023—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13227592HCID 13227592—

Reaction Conditions

Temperature-75 °C

Reaction Steps

A solution of n-butyllithium in hexanes (1.6M, 26 ml) was added with stirring to a solution of diisopropylamine (6.2 ml) in tetrahydrofuran (8 ml) at below -25° C. under nitrogen. After 30 min, the mixture was cooled to -75° C. and ethyl cyclopropylacetate (4.5 g) added dropwise keeping the temperature below -65° C. The mixture was then maintained below -75° C. for 3 h before chlorotrimethylsilane (3.8 ml) was added below -65° C. The reaction was allowed to warm to ambient temperature and then evaporated to dryness. The residue was slurried with hexane and filtered. The filtrate was evaporated to an orange oil which was distilled in vacuo to give the title compound (4.0 g) as a clear mobile liquid, b.p 80-82° C., 3×10-2 bar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994344
Source datasetuspto-grants-1999_11
ORD IDord-b6e1c081b6054ceba5f3d3e7115f5d9f
Source noteuspto-grants-1999_11