HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829902Generated: October 26, 2026
Water → Ethyl 3-[(trimethylsilyl)oxy]but-2-enoate
https://huagongshe.com/reaction/1829902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Ethyl 3-[(trimethylsilyl)oxy]but-2-enoate | HCID 54340571 | 106.4% |
Reaction Steps
182.21 g (1.4 mol) of ethyl acetoacetate and 169.98 g (1.4 mol) of triethylamine were dissolved in a mixed solvent of 182 mL of tetrahydrofuran and 1.64 L of hexane under nitrogen atmosphere. To this solution, 167.3 g (1.54 mol) of trimethylsilyl chloride was added dropwise at a temperature of 21 to 45° C., and then the solution was stirred at 25° C. for 3 hours. The reaction mixture was cooled to 10° C., the reaction was ceased by adding 547 mL of water thereto and an organic layer was separated. The organic layer was washed two times with 273 mL of water, dried over 54.7 g of anhydrous magnesium sulfate, and then filtered. The solvent was evaporated to obtain 301.3 g (crude yield 106.4%) of 3-(trimethylsilyloxy) but-2-enoic acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07064209B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-b421707507ed498d8d871748c38273a5 |
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| Source note | uspto-grants-2006_06 |
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