HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 18960336, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | HCID 18960345 | HCID 18960345 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Trimethyl orthoformate | HCID 9005 | — |
| Product | HCID 18960336 | HCID 18960336 | — |
Reaction Steps
Three g (9 mmol) of 2,3-bis-tert.-butoxycarbonyloxy-benzaldehyde were dissolved at room temperature in 10 ml of methanol and 1.2 ml of trimethyl orthoformate. For complete dissolution of the benzaldehyde derivative, 1.5 ml of toluene were added. This was followed by the addition of 3.75 mg of RhCl3 [CH3C(CH2PPh2)3 ] as catalyst. The mixture was then stirred overnight at room temperature. The solvents were separated off by steam distillation and the oily residue was taken up in a little toluene. The undissolved rhodium catalyst was filtered off over a G-4 frit. After the toluene had been stripped off under reduced pressure, the product was dried in an oil pump vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05356752 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-530afe2a2df14a12a854afdb63032089 |
| Source note | uspto-grants-1994_10 |