HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490364Generated: October 30, 2026
Imidazole → Tri-isopropyl-(2-trifluoromethyl-furan-3-ylmethoxy)-silane
https://huagongshe.com/reaction/490364
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Triisopropylsilyl chloride | HCID 139400 | — |
| Reactant | (2-Trifluoromethyl-furan-3-yl)-methanol | HCID 17953606 | — |
| Reactant | 2-(2-Methylfuran-3-yl)ethan-1-ol | HCID 18444636 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tri-isopropyl-(2-trifluoromethyl-furan-3-ylmethoxy)-silane | HCID 18444682 | — |
Reaction Steps
A solution of the (2-trifluoromethyl-furan-3-yl)-methanol from (i) in dry dichloromethane (180 ml) was treated with chloro-tri-isopropyl-silane (2.6 g, 13.4 mmoles) and imidazole (1.45 g, 21.3 mmoles) and the mixture was stirred overnight at room temperature. Further aliquots of chloro-tri-isopropyl-silane (0.9 g, 4.64 mmoles) and imidazole (0.5 g, 7.34 mmoles) were added and the mixture was stirred for 3 h. The reaction mixture was diluted with water, the organic phase separated and washed sequentially with 0.1M aqueous hydrochloric acid, water, saturated aqueous sodium bicarbonate, water and brine. After drying, evaporation of the solvents afforded a colourless oil. The oil was distilled under reduced pressure (0.05 torr) in a Kugelruhr apparatus collecting the fraction boiling at an oven temperature of 125±20° C. to afford compound 88 as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528157B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-07ad163b6cf849129ecc6c24c453d60a |
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| Source note | uspto-grants-2009_05 |
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