HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247661Generated: October 26, 2026
Carbon Tetrachloride → 2-(4-Ethoxyphenyl)-2-methyl-2-silapropyl acetate
https://huagongshe.com/reaction/247661
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Silane, (chloromethyl)(4-ethoxyphenyl)dimethyl- | HCID 184717 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(4-Ethoxyphenyl)-2-methyl-2-silapropyl acetate | HCID 14014483 | 105.4% |
Reaction Steps
In a flask under nitrogen were placed 10.1 g (0.044 mole) of (chloromethyl)(4-ethoxyphenyl)dimethylsilane, 4.0 g (0.049 mole) of sodium acetate, 1.2 g (0.0043 mole) of tetrabutylammonium chloride, and 75 ml of carbon tetrachloride. This mixture was refluxed for four days. After cooling to room temperature, 2.0 g (0.024 mole) of sodium acetate and 0.60 g (0.0022 mole) of tetrabutylammonium chloride was added, and the reaction mixture was refluxed for five more days. This mixture was then diluted with diethyl ether, filtered through silica gel, and the solvent was evaporated under reduced pressure, leaving 11.7 g of 2-(4-ethoxyphenyl)-2-methyl-2-silapropyl acetate as a clear, light brown oil. The nmr spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04709068 |
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| Source dataset | uspto-grants-1987_11 |
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| ORD ID | ord-c5694bf43ac44a9f9d99458ce32adaab |
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| Source note | uspto-grants-1987_11 |
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