HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430249Generated: October 31, 2026
2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl → HCID 89498037, compound
https://huagongshe.com/reaction/1430249
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl | HCID 16217985 | — |
| Reactant | HCID 89498113 | HCID 89498113 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 89498037 | HCID 89498037 | — |
Reaction Steps
A mixture of EXAMPLE 107A (60 mg), dicyclohexyl(2′,6′-diisopropoxybiphenyl-2-yl)phosphine (RuPhos, 4.58 mg) and tris(dibenzylideneacetone)dipalladium(0) (2.25 mg) in tetrahydrofuran (0.5 mL) and 1-methyl-2-pyrrolidinone (0.5 mL) was stirred at room temperature for 5 minutes while bubbling N2 through the reaction mixture. To this solution was added 0.5 M (cyclohexylmethyl)zinc(II) bromide (0.393 mL) at room temperature. The reaction mixture in a sealed tube was heated in a preheated oil bath at 100° C. overnight and cooled. The reaction mixture was quenched with water and diluted with dichloromethane. The dichloromethane layer was washed with water and concentrated. The residue was purified by flash chromatography, and eluted with 5% ethyl acetate in dichloromethane to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940737B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-7d48417cd7204e37acee401f9e94f97d |
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| Source note | uspto-grants-2015_01 |
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