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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482641Generated: October 26, 2026

Chlorotrimethylsilane → Trimethylsilyl dibutylphosphinite

https://huagongshe.com/reaction/482641

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 l 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 a 80° C. (1.5 mmHg) afforded 4.1 g (86%) of the desired product. 1H NMR (CDCl3) δ1.8-1.2 (m, 6H), 1.1-0.7 (m, 3H), 0.17 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04574060
Source datasetuspto-grants-1986_03
ORD IDord-9942bdc590ec49c9af7f2405c35bb393
Source noteuspto-grants-1986_03