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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 5-Methoxyindan-1-one | HCID 78787 | — |
| Reactant | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Water methylene chloride | HCID 21908982 | — |
| Product | 5-methoxy-1-(trifluoromethyl)-2,3-dihydro-1H-inden-1-ol | HCID 18677646 | 73.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329396B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-da738617294547719878d5fd96b6b3d4 |
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| Source note | uspto-grants-2001_12 |
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