HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482641Generated: October 26, 2026
Chlorotrimethylsilane → Trimethylsilyl dibutylphosphinite
https://huagongshe.com/reaction/482641
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Diethylphosphite | HCID 3780918 | — |
| Reactant | HCID 178418682 | HCID 178418682 | — |
| Reactant | HCID 178454905 | HCID 178454905 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Trimethylsilyl dibutylphosphinite | HCID 12651389 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04574060 |
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| Source dataset | uspto-grants-1986_03 |
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| ORD ID | ord-9942bdc590ec49c9af7f2405c35bb393 |
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| Source note | uspto-grants-1986_03 |
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