HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643589Generated: October 30, 2026
Tri-o-tolylphosphine → HCID 67302023, compound
https://huagongshe.com/reaction/643589
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Methyl 2-acetamidoacrylate | HCID 98644 | — |
| Reactant | 5-Bromo-2-chloro-m-xylene | HCID 2735555 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 67302023 | HCID 67302023 | — |
Reaction Steps
Under a nitrogen atmosphere 30.0 g (136.7 mmol) 5-bromo-2-chloro-1,3-dimethylbenzene, 24.0 g (164.0 mmol) methyl 2-acetylamino-acrylate in 420 mL triethylamine and 200 mL acetonitrile were combined with 3.4 g (10.9 mmol) tri-o-tolyl-phosphane and 2.4 g (10.9 mmol) Pd(OAc)2 and stirred for 18 h at 80° C. The precipitate was suction filtered, the filtrate was evaporated down i. vac., combined with 800 mL DCM and 800 mL water, the organic phase was separated off and dried over Na2SO4. After the desiccant and solvent had been eliminated the residue was stirred with EtOAc, suction filtered and dried i. vac.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700598B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-106f33c3f3674f26ab4d166b7041d976 |
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| Source note | uspto-grants-2010_04 |
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