HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265440Generated: October 26, 2026
Lithium Chloride → Methyl 1,1-dimethyl-3-phenyl-1H-indene-5-carboxylate
https://huagongshe.com/reaction/265440
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Tributylphenyltin | HCID 607632 | — |
| Reactant | Methyl 1,1-dimethyl-3-(trifluoromethanesulfonyloxy)-1H-indene-5-carboxylate | HCID 19034466 | — |
| Catalyst | Triphenylarsine | HCID 11773 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 1,1-dimethyl-3-phenyl-1H-indene-5-carboxylate | HCID 19034436 | 83.1% |
Reaction Steps
Methyl 1,1-dimethyl-3-(trifluoromethanesulfonyloxy)-1H-indene-5-carboxylate (580 mg, 1.86 mmol), tris(dibenzylideneacetone)dipalladium (0) (Pd2 dba3, 17 mg, 0.02 mmol), triphenylarsine (46 mg, 0.15 mmol), lithium chloride (240 mg, 5.59 mmol) and phenyltributyltin (680 mg, 1.86 mmol) in 5 mL of 2-methyl pyrrolidinone were stirred at 55° C. for 1.5 days. The mixture was diluted with water (30 mL), and extracted with ethyl ether (30 mL×3). The combined extracts were dried over magnesium sulfate and evaporated. The residue was purified by flash chromatography (EtOAc:hexane=1:20 to 1:5) to give 0.43 g (83% yield) of the title compound as a white solid; 1H-NMR (CDCl3) δ 1.41 (s, 6H), 3.91 (s, 3H), 6.48 (s, 1H), 7.39-7.62 (m, 6H), 7.99 (d, J=6.8 Hz, 1H), 8.14 (s, 1H); MS m/e 279 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05648385 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-27b6995ad0f54a5f96f6bad701cc368f |
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| Source note | uspto-grants-1997_07 |
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