Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 3-Methoxy-2-methylbenzaldehyde | HCID 13162663 | — |
| Product | HCID 59370485 | HCID 59370485 | — |
Reaction Steps
To a solution of 2-methyl-3-(methyloxy)benzaldehyde (available from Allichem Product List; 20 g; 133 mmol) in nitromethane (400 ml) was added ammonium acetate (6.16 g; 80 mmol) and the resulting orange mixture was stirred for 1 h at 100° C. then cooled to room temperature and concentrated in vacuo. The residue was partitioned between ethyl acetate (×2) and brine, and the organic layers washed with brine, dried (MgSO4) and concentrated in vacuo. Trituration with dichloromethane/ether gave the title compound as a yellow solid (6.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08278324B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-1ad402ef4553450eb68a79476034f90c |
|---|
| Source note | uspto-grants-2012_10 |
|---|