HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalaldehyde → HCID 71434730, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalaldehyde | HCID 4807 | — |
| Reactant | (Triphenylphosphoranylidene)acetonitrile | HCID 85524 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71434730 | HCID 71434730 | 14.2% |
Reaction Steps
A solution of triphenylphosphoranylidene acetonitrile (13 g) in dry dichloromethane (20 ml) was added to a solution of ortho phthalaldehyde (5.4 g) in dry dichloromethane (20 ml), at 0°. The solution was stirred at room temperature for 1 h, then the solvent evaporated and the oil taken up with diethyl ether. The solid was filtered, washed with ether and the solution evaporated to dryness to give a yellow oil, which was eluted on a silica gel column (gradient petrol ether/diethyl ether, 1:1) to give the (E)-isomer of the title compound (0.9 g) and the (Z)-isomer of the title compound (2 g) (eluted first) as white solids which were recrystallized from petrol ether/diethyl ether (9:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04946851 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-7c4c4f20088943518d4c15fb43ed5d8c |
| Source note | uspto-grants-1990_08 |