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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269269Generated: October 30, 2026

Hydrochloric Acid → 5-methoxy-1-(trifluoromethyl)-2,3-dihydro-1H-inden-1-ol

https://huagongshe.com/reaction/2269269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant5-Methoxyindan-1-oneHCID 78787—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
SolventTetrahydrofuranHCID 8028—
SolventWater methylene chlorideHCID 21908982—
Product5-methoxy-1-(trifluoromethyl)-2,3-dihydro-1H-inden-1-olHCID 1867764673.3%

Reaction Steps

To a stirred solution of 5-methoxy-1-indanone (1.00 g, 6.17 mmol) and trifluoromethyltrimethylsilane (1.32 g, 9.26 mmol) in dry THF (15 ml) was added 1.0M THF solution of tetrabutylammonium fluoride (0.05 ml) with ice-cooling.The reaction mixture was stirred at room temperature for 21 h. To a mixture was 1N HCl (20 ml). and stirred at room temperature for 25 h. The reaction mixture was diluted with CH2Cl2-water. The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined solution was washed with water and brine, dried (MgSO4) and concentrated in vacuo to give crude product as a dark yellow oil. The crude product was purified by column chromatography on silica gel with hexane-ethyl acetate(5:1-3:1) to give Compound 62 (1.05 g, 73%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329396B1
Source datasetuspto-grants-2001_12
ORD IDord-da738617294547719878d5fd96b6b3d4
Source noteuspto-grants-2001_12