HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731197Generated: October 25, 2026
Ethyl trimethylsilylacetate → Ethyl 3-(1-methyl-1H-imidazol-5-yl)-3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)acrylate
https://huagongshe.com/reaction/731197
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl trimethylsilylacetate | HCID 77687 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | (1-Methyl-1H-imidazol-5-yl)(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)methanone | HCID 57835849 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-(1-methyl-1H-imidazol-5-yl)-3-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)acrylate | HCID 68686278 | 118.4% |
Reaction Steps
To a solution of lithium bis(trimethylsilyl)amide (6.8 mmol, 1 M in THF) was added ethyl trimethylsilylacetate (6.5 mmol) dropwise at −78° C. After 20 minutes at −78° C., a solution of 74.2 (5.9 mmol) in THF (20 mL) was added dropwise. The reaction was maintained at −78° C. for 3 hours and at −45° C. for 2 hours. The reaction was quenched with saturated NH4Cl (aq) at 0° C. and warmed to room temperature. The mixture was extracted with EtOAc (500 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to afford crude 74.3 (2.49 g). MS ESI (pos.) m/e 357.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582803B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-d76b189b63724601a6cd10248700550d |
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| Source note | uspto-grants-2009_09 |
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