HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283430Generated: October 27, 2026
Chlorotrimethylsilane → (1-Isobutoxy-2-methyl-propenyloxy)-trimethyl-silane
https://huagongshe.com/reaction/2283430
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Isobutyl isobutyrate | HCID 7351 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-Isobutoxy-2-methyl-propenyloxy)-trimethyl-silane | HCID 15626276 | 77.8% |
Reaction Steps
Step 1 To a solution of diisopropylamine (2.94 mL, 20.8 mmol) in THF (20 mL) under nitrogen at 0° C. was added nBuLi (2.5M in hexanes, 8.32 mL, 20.8 mmol, 1 eq.) and the solution stirred at 0° C. for 30 min. The solution was cooled to −78° C. and then a solution of isobutylisobutyrate (3.49 mL, 20.8 mmol) in THF (6 mL) was added dropwise and then the reaction stirred at −78° C. for 1 h. TMS-Cl (3.19 mL, 25 mmol) was then added dropwise and the reaction allowed to warm to room temperature over 3 h. The reaction was quenched with ice-water (20 mL) and EtOAc (20 mL) was added. The organic phase was washed with water (10 mL) and then brine (10 mL) before it was dried (MgSO4), filtered and concentrated to give (1-isobutoxy-2-methyl-propenyloxy)-trimethyl-silane (3.5 g) used crude in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145354B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-0a0157e6eee140748b6d58787acb1562 |
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| Source note | uspto-grants-2015_09 |
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