HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898768Generated: October 25, 2026
Tributylphosphine → HCID 21867689, compound
https://huagongshe.com/reaction/898768
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 3,4-Dimethoxyphenol | HCID 16251 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | 4-(1-Hydroxy-3-butenyl)benzonitrile | HCID 11019345 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21867689 | HCID 21867689 | 68.6% |
Reaction Steps
A cooled (0° C.) mixture of 4-(1-hydroxy-3-butenyl)benzonitrile (14.6 g, 84.3 mmol) and 3,4-dimethoxyphenol (19.5 g, 125.4 mmol) in toluene is (500 mL) was treated with tributylphosphine (32.14 mL of 97% purity, 25.6 g, 126.4 mmol), followed by 1,1′-(azodicarbonyl)dipiperidine (31.8 g, 126.4 mmol). After addition was complete, the reaction mixture thickened and the temperature rose to 15° C. Additional toluene was added (500 mL), and the mixture stirred at rt overnight. The precipitate of tributylphosphine oxide was then removed by filtration and the filtrate concentrated in vacuo to give 65.8 g of crude product. This was purified by chromatography on silica gel, eluting with toluene:methanol (98:2), to yield 17.9 g of the sub-title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07351821B2 |
|---|
| Source dataset | uspto-grants-2008_04 |
|---|
| ORD ID | ord-16087b2406c44ba1af1bb931444bc64d |
|---|
| Source note | uspto-grants-2008_04 |
|---|