HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitrobenzaldehyde → 4-Isopropyl-2-(trans-3-nitrostyryl)thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Methyl-4-(1-methylethyl)thiazole | HCID 520569 | — |
| Product | 4-Isopropyl-2-(trans-3-nitrostyryl)thiazole | HCID 15718358 | 32% |
Reaction Steps
To 11.3 ml of acetic anhydride were added 29.0 g of 3-nitrobenzaldehyde and 27.1 g of 4-isopropyl-2-methylthiazole and the reaction was carried out under nitrogen gas stream at 170° C. for 23 hours. After completion of the reaction, low boiling materials were evaporated under reduced pressure and the residue was recrystallized from ethyl ether-n-hexane to give 16.8 g (yield 32%) of the title compound as yellowish white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04902700 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-37b0ac1afc514b0aa30310eae7c1b74b |
| Source note | uspto-grants-1990_02 |