HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376051Generated: November 1, 2026
Chlorotrimethylsilane → HCID 178476819, compound
https://huagongshe.com/reaction/376051
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Phosphinic Acid | HCID 4124402 | — |
| Reactant | HCID 178460913 | HCID 178460913 | — |
| Reactant | HCID 178476775 | HCID 178476775 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178476819 | HCID 178476819 | — |
Reaction Steps
Hypophosphorous acid (100%, 2.0 g, 0.03M) and ethyl chloroformate (3.3 g, 0.03M) are stirred under nitrogen at room temperature in THF (40 ml). Triethylamine (3.03 g, 0.03M) is carefully added with cooling over 1 hour. 31P nmr shows that there is 85% conversion to ethyl hypophosphite (31P nmr δ=16 ppm). Trimethylsilyl chloride (3.3 g, 0.3M) is added followed by triethylamine (3.03 g, 0.03M). The mixture is stirred for 1 hour, when conversion to ethyltrimethylsilyl phosphinate (31P nmr δ=149 ppm) is complete. Acetone (5 ml) is added and the mixture is stirred for 1 hour at 60° C. The mixture is then cooled, quenched with water and washed with methylene chloride. The aqueous phase is evaporated and the residual gum is stirred with ether. Evaporation of the ether gives ethyl (1-hydroxy-1-methylethyl)phosphinate after distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05488171 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-997bd79b8ebb47db98978c40011094bf |
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| Source note | uspto-grants-1996_01 |
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