HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993879Generated: October 30, 2026
Triacetoxyperiodinane → HCID 18185015, compound
https://huagongshe.com/reaction/1993879
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | 5-Trifluoromethyl-indan-2-yl-methanol | HCID 66877512 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18185015 | HCID 18185015 | 98% |
Reaction Steps
The above 5-trifluoromethyl-indan-2-yl-methanol (216 mg, 1 mmol) was dissolved in methylene chloride (15 mL) and the solution was cooled in an ice bath. To this solution was added Dess-Martin reagent (450 mg, 1.06 mmol) in four portions. The mixture was warmed to room temperature and stirred for 1 hr. The mixture was evaporated to dryness and the residue was triturated with petroleum ether (14 mL) and ether (7 mL). The precipitate was filtered out and the filtrate was extracted with ether and sodium bicarbonate solution. The organic layer was dried over sodium sulfate and solvents were evaporated to give 5-trifluoromethyl-indan-2-carbaldehyde (210 mg) as pale green oil. 1H-NMR (CDCl3) □ 9.78 (s, 1H), 7.48 (s, 1H), 7.43 (d, 1H), 7.32 (d, 1H), 3.33-3.38 (m, 3H), 3.15-3.27 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652053B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-c025d9911ba5488c975d39755884a3b3 |
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| Source note | uspto-grants-2010_01 |
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