HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371Generated: October 23, 2026
Tri-o-tolylphosphine → Ethyl (E)-4-[-2-(5,6-dihydro-5,5-dimethyl-8-(ethylthio)-naphthalen-2-yl)ethenyl]benzoate
https://huagongshe.com/en/reaction/1371
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Ethyl 4-vinylbenzoate | HCID 10866858 | — |
| Reactant | 2-Bromo-5,6-dihydro-5,5-dimethyl8-(ethylthio)-naphthalene | HCID 22571521 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl (E)-4-[-2-(5,6-dihydro-5,5-dimethyl-8-(ethylthio)-naphthalen-2-yl)ethenyl]benzoate | HCID 86586452 | — |
Reaction Steps
To a degassed solution of 0.50 g (1.7 mmol) of 2-bromo-5,6-dihydro-5,5-dimethyl-8-(ethylthio)-naphthalene (Compound A36) and 0.45 g (2.5 mmol) of ethyl 4-vinylbenzoate in 4.0 mL of triethylamine, was added 109 mg (0.36 mmol) of tri-o-tolylphosphine and then 35 mg (0.16 mmol) of palladium(II) acetate. The reaction was heated at 90° C. for 2.25 h. The reaction was concentrated in vacuo and purified by flash chromatography (silica, 2% ethyl acetate in hexane) to afford the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05723666 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-b1bd58830652436484aeb0d21b29efe6 |
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| Source note | uspto-grants-1998_03 |
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