HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521601Generated: October 30, 2026
Tricyclohexylphosphine → HCID 70976931, compound
https://huagongshe.com/reaction/1521601
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reactant | HCID 59619900 | HCID 59619900 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 70976931 | HCID 70976931 | — |
Reaction Steps
To a vial containing the title compound from Example 53 Step H (0.10 g, 0.39 mmol), bis(pinacolato)diboron (0.12 g, 0.47 mmol), tris(dibenzylideneacetone)dipalladium (0) (0.035 g, 0.039 mmol), tricyclohexylphosphine (0.022 g, 0.077 mmol) and potassium acetate (0.114 g, 1.16 mmol) was added 1,4-dioxane (3.9 mL). The reaction was heated to 80° C. for 16 hours. It was then cooled to room temperature, passed through a syringe filter, and concentrated under reduced pressure to afford the title compound: LCMS m/z 224.19 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073929B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-4f0b534500954174b7d3c0a8a485c60d |
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| Source note | uspto-grants-2015_07 |
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