HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324003Generated: October 25, 2026
Ethyl isovalerate → (1-Ethoxy-3-methyl-but-1-enyloxy)-triisopropyl-silane
https://huagongshe.com/reaction/324003
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl isovalerate | HCID 7945 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triisopropylsilyl trifluoromethanesulfonate | HCID 2724529 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Solvent | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Product | (1-Ethoxy-3-methyl-but-1-enyloxy)-triisopropyl-silane | HCID 53927273 | — |
Reaction Steps
Tetrahydrofuran (100 ml) and 1,3-dimethyl-3,4,5,6-tetrahydro 2 (1H)-pyrimidinone (140 ml) were mixed at −20° C. and lithium bis (trimethylsilyl) amide (1M in tetrahydrofuran, 100 ml) was added. The mixture was cooled to −70° C., ethyl isovalerate (18.75 ml) added and stirred for ½ hour at −70° C. Triisopropylsilyl trifluoromethane sulfonate was added and the mixture left to stir at −75° C. for ½ hour before warming to room temperature and stirring for 3 hours. The reaction mixture was quenched with aqueous sodium bicarbonate (8%, 150 ml) and extracted with hexane (1000 ml). The hexane extract was washed with water (4×500 ml), dried (MgSO4), filtered and concentrated in vacuo to afford a crude yellow oil containing the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06215002B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-7bdf0bcac9b34bd9a369e584d6237570 |
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| Source note | uspto-grants-2001_04 |
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