HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106042Generated: November 1, 2026
(Trifluoromethyl)trimethylsilane → HCID 57809779, compound
https://huagongshe.com/reaction/2106042
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 57809946 | HCID 57809946 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57809779 | HCID 57809779 | 105.7% |
Reaction Steps
To 1.7 g (8.16 mmol) of (6-fluoro-4-methylchroman-4-yl)acetaldehyde and 1.69 mL (11.4 mmol) of trimethyl(trifluoromethyl)silane in 15 mL of tetrahydrofuran was added 1 mL (1 mmol) of a 1M solution of tetrabutylammonium fluoride in tetrahydrofuran. The mixture stirred for 1 hour and then an additional 9 mL (9 mmol) of a 1M solution of tetrabutylammonium fluoride in tetrahydrofuran was added. After 18 hours, the mixture was concentrated in vacuo and diluted with 1N aqueous HCl and extracted with three 50 mL portions of diethyl ether. The combined organic layers were dried over magnesium sulfate and concentrated in vacuo to afford 2.4 g of crude 1,1,1-trifluoro-3-(6-fluoro-4-methylchroman4-yl)propan-2-ol as a mixture of diastereomers. The crude oil was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07579469B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-55f1c2fa963540a6aa435b0ea167ecd4 |
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| Source note | uspto-grants-2009_08 |
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