HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199848Generated: October 29, 2026
Hexafluoroacetone → HCID 117940104, compound
https://huagongshe.com/reaction/2199848
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexafluoroacetone | HCID 12695 | — |
| Reactant | HCID 117940114 | HCID 117940114 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117940104 | HCID 117940104 | 15.5% |
Reaction Steps
To a stirred solution of 2-(2-chloro-5-(trifluoromethyl)benzyl)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one 269 (0.1 g, 0.226 mmol) in dry THF, cooled to 0° C., n-BuLi (0.021 g, 0.339 mmol) was added drop wise and the solution stirred for 10 min. Then hexafluoroacetone 244 (0.10 g, 0.453 mmol) was added to the reaction and stirred for another 2 h. After completion of the reaction, it was quenched with saturated ammonium chloride solution. The organic layer was separated and aqueous phase was extracted again with diethyl ether, the combined organic layer was dried over sodium sulphate and concentrated to get the crude 270, which was purified through 100-200 mesh silica gel by eluting with 15% ethyl acetate in hexane to give 20 mg of compound 2-(2-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-5-(trifluoromethyl)benzyl)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one 270.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359315B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-50b067141f4d4634bbf34c443013b972 |
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| Source note | uspto-grants-2016_06 |
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