HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809407Generated: October 26, 2026
Imidazole → 2,2-Dimethyl-3-triisopropylsilanyloxy-propionic acid methyl ester
https://huagongshe.com/reaction/1809407
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Methyl 3-hydroxypivalate | HCID 84152 | — |
| Reactant | Triisopropylsilyl chloride | HCID 139400 | — |
| Solvent | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Product | 2,2-Dimethyl-3-triisopropylsilanyloxy-propionic acid methyl ester | HCID 59267974 | 86.7% |
Reaction Steps
To a solution of 6.76 mL (53 mmol) of methyl 2,2-dimethyl-3-hydroxypropionate in anhydrous THF/DMF (110 mL, 10/1) are added 4.33 g (63.6 mmol) of imidazole and 11.3 mL (53 mmol) of chlorotriisopropylsilane under nitrogen atmosphere. After stifling at room temperature for 20 h, the reaction mixture is concentrated under reduced pressure and the residue is dissolved in TBME (175 mL). The organic layer is washed with water (30 mL), brine (30 mL), dried over Na2SO4 and filtered. The filtrate is concentrated under reduced pressure to afford 13.25 g of 2,2-dimethyl-3-triisopropylsilanyloxy-propionic acid methyl ester as a yellow oil, which is used in the next step without further purification. Yield: 79%; 1H NMR (500 MHz, CHLOROFORM-d) δ ppm 1.01-1.07 (21H, m), 1.18 (6H, s), 3.66 (3H, s), 3.69 (2H, s)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362039B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-b628f83a9da3464fa716912aa64f7b09 |
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| Source note | uspto-grants-2013_01 |
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