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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106042Generated: November 1, 2026

(Trifluoromethyl)trimethylsilane → HCID 57809779, compound

https://huagongshe.com/reaction/2106042

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 57809946HCID 57809946—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57809779HCID 57809779105.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579469B2
Source datasetuspto-grants-2009_08
ORD IDord-55f1c2fa963540a6aa435b0ea167ecd4
Source noteuspto-grants-2009_08