HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → alpha-Methylcinnamic alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Phenyl-2-methylacrolein | HCID 5354896 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | alpha-Methylcinnamic alcohol | HCID 6393846 | 94% |
Reaction Steps
Into a stainless steel autoclave equipped with a glass inner tube, Cu(NO3)(PPh3)2 (11.7 mg, 0.018 mmol) and triphenylphosphine (28.3 mg, 0.108 mmol) were introduced. The inside of the autoclave was then replaced with nitrogen. To the autoclave, an ethanolic solution of sodium hydroxide (0.03 M) (6.0 mL, 0.18 mmol) and α-methyl cinnamic aldehyde (1.26 mL, 9 mmol) were added, and stirring was performed at a hydrogen pressure of 5 MPa at 50° C. for 16 hours. The hydrogen was released with great care, and the conversion was analyzed by GC (>99%). The contents were concentrated, and then purified by silica gel chromatography. Thus, 1.25 g of the α-methyl cinnamic alcohol was obtained (yield: 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08697881B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-3082572c50a94bb6a7db673e916b7932 |
| Source note | uspto-grants-2014_04 |