HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467919Generated: October 26, 2026
Triphenylphosphine → 6-(3,3,3-trifluoropropoxy)-2,3-dihydro-1H-inden-1-one
https://huagongshe.com/reaction/1467919
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 3,3,3-Trifluoro-1-propanol | HCID 137512 | — |
| Reactant | 6-Hydroxy-1-indanone | HCID 7020659 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(3,3,3-trifluoropropoxy)-2,3-dihydro-1H-inden-1-one | HCID 67979342 | 22% |
Reaction Steps
To a solution of 6-hydroxy-2,3-dihydro-1H-inden-1-one (3.0 g, 20.3 mmol) in THF (140 mL) were triphenylphosphine (7.97 g, 30.4 mmol) and 3,3,3-trifluoropropan-1-ol (1.96 mL, 22.3 mmol) added. Diisopropyl azodicarboxylate (5.98 mL, 30.4 mmol) was added dropwise and the mixture was left stirring at r.t. overnight. Since there was starting material remaining, 3,3,3-trifluoro-1-propanol (0.892 mL, 10.1 mmol) was added dropwise and stirring was continued. After 30 min the mixture was heated to 40° C. and after 1 h the mixture was concentrated. The product was purified by flash chromatography (0-12% EtOAc in heptane as eluent) to afford 1.08 g (22% yield) of the title compound (containing some diisopropyl azodicarboxylate): 1H NMR (500 MHz, CDCl3) δ 2.65 (qt, 2 H), 2.71-2.77 (m, 2 H), 3.05-3.13 (m, 2 H), 4.23 (t, 2 H), 7.17-7.23 (m, 2 H), 7.40 (d, 1 H); MS (ES+) m/z 245 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09000182B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-84f43b035cf948fbb69a1e590e5b0a70 |
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| Source note | uspto-grants-2015_04 |
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