HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62263Generated: October 25, 2026
p-Toluenesulfonic acid → (E)-5-bromo-6-methoxy-2-(4-((trifluoromethyl)thio)benzylidene)-2,3-dihydro-1H-inden-1-one
https://huagongshe.com/reaction/62263
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-[(Trifluoromethyl)sulfanyl]benzaldehyde | HCID 2777846 | — |
| Reactant | 5-Bromo-6-methoxy-1-indanone | HCID 22278718 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (E)-5-bromo-6-methoxy-2-(4-((trifluoromethyl)thio)benzylidene)-2,3-dihydro-1H-inden-1-one | HCID 117940068 | — |
Reaction Steps
To a solution of 11 (250 mg, 1.04 mol) in toluene 15 mL was added 4-((trifluoromethyl)thio)benzaldehyde 72 (235 mg, 1.144 mol). PTSA (357 mg, 2.08 mol) was added, the reaction mixture stirred at 120° C. for 6 h, diluted with ethyl acetate and washed with water (3×25 mL). The organic layer was dried over sodium sulphate and concentrated to get the crude compound 104 and was purified through flash chromatography by using 100-200 mesh silica gel. The resulting compound (E)-5-bromo-6-methoxy-2-(4-((trifluoromethyl) thio)benzylidene)-2,3-dihydro-1H-inden-1-one 104 was eluted at 10% ethyl acetate in hexane to afford yellow coloured solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09446047B2 |
|---|
| Source dataset | uspto-grants-2016_09 |
|---|
| ORD ID | ord-1e3f31e2c0984332bb4cd5f97f7c36ac |
|---|
| Source note | uspto-grants-2016_09 |
|---|