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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073603Generated: November 1, 2026

Chlorotrimethylsilane → HCID 14371698, compound

https://huagongshe.com/reaction/2073603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantSodium BromideHCID 253881—
ReactantHCID 14371697HCID 14371697—
SolventAcetonitrileHCID 6342—
ProductHCID 14371698HCID 1437169863.6%

Reaction Steps

2 g (4.5 millimoles) of diethyl (E)-4-[2(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-1propenyl]-benzenephosphonate, 1.86 g (18 millimoles) of sodium bromide and 3 g (27 millimoles) of trimethylchlorosilane in 10 ml of acetonitrile were stirred for 3 hours at 40° C. The mixture was then allowed to cool and was filtered, and the filtrate was evaporated down. The oil which remained was stirred for 30 minutes with water at room temperature and then extracted with ether, and the organic phase was washed with water, dried over sodium sulfate and evaporated down. Recrystallization of the residue from ethyl acetate gave 1.1 g of the title compound of melting point 208°-209° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04918212
Source datasetuspto-grants-1990_04
ORD IDord-ed09cfba7f9545a992065df2b142317f
Source noteuspto-grants-1990_04