HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199840Generated: October 29, 2026
p-Toluenesulfonic acid → HCID 117940031, compound
https://huagongshe.com/reaction/2199840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Hexafluoroacetone | HCID 12695 | — |
| Reactant | HCID 117940146 | HCID 117940146 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 117940031 | HCID 117940031 | — |
Reaction Steps
To a stirred solution of 255 (0.05 g, 0.142 mmol) in toluene was added PTSA (0.054 g, 0.284 mmol) and kept stirring at 120° C. Hexafluoroacetone 244 (0.078 g, 0.356 mmol) was added to the reaction and kept at temperature and stirred for 16 h. Reaction was then cooled to RT, diluted with water, and extracted with ethyl acetate twice, The organic layer was dried over sodium sulphate and concentrated to get the crude, which was purified through flash chromatography by using 100-200 mesh silica gel and eluting the compound at 30% ethyl acetate in hexane as thick sticky solid 2-((5-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)pyridin-3-yl)methyl)-6-methoxy-5-(4-methylpiperazin-1-yl)-2,3-dihydro-1H-inden-1-one 256.
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-7b549695dff44d4d8f406a1f3198b86a |
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| Source note | uspto-grants-2016_06 |
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