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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isovalerateHCID 7945—
ReactantTetrahydrofuranHCID 8028—
ReactantTriisopropylsilyl trifluoromethanesulfonateHCID 2724529—
ReactantLithium HexamethyldisilazideHCID 2733832—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Product(1-Ethoxy-3-methyl-but-1-enyloxy)-triisopropyl-silaneHCID 53927273—

Reaction Conditions

Temperature-70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06215002B1
Source datasetuspto-grants-2001_04
ORD IDord-7bdf0bcac9b34bd9a369e584d6237570
Source noteuspto-grants-2001_04