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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986083Generated: October 30, 2026

Chlorotrimethylsilane → Trimethylsilyl dibutylphosphinite

https://huagongshe.com/reaction/986083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDiethylphosphiteHCID 3780918—
ReactantHCID 178418682HCID 178418682—
ReactantHCID 178454905HCID 178454905—
SolventTolueneHCID 1140—
SolventTriethylamineHCID 8471—
ProductTrimethylsilyl dibutylphosphiniteHCID 1265138986%

Reaction Conditions

Temperature80 °C

Reaction Steps

The procedure described in Tetrahedron, 1967, 23, 1065 (M. Grayson et al.) was followed. Dibutylphosphine oxide, prepared from butyl magnesium bromide and diethylphosphite, (3.3 g, 20 mmol) and triethylamine (2.02 g, 20 mml) were dissolved in toluene (20 mL) and treated with a solution of trimethylsilyl chloride (2.17 g, 20 mmol) in toluene (5 mL) at room temperature. The solution got very warm and a precipitate formed immediately. The mixture was heated at 80° C. for two hours, then filtered, washed with toluene, and concentrated. Kugelrohr distillation at 80° C. (1.5 mmHg) afforded 4.1 g (86%) of the desired product. 1H NMR (CDCl3) δ 1.8-1.2 (m, 6 H), 1.1-0.7 (m, 3 H), 0.17 (s, 9 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04710545
Source datasetuspto-grants-1987_12
ORD IDord-8c05fd1ab3224d5481a7a4e4253ee0ac
Source noteuspto-grants-1987_12