HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indole, 6-methyl- → Alpha-nitro-6-methyl-3-indoleacrylic acid methylester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indole, 6-methyl- | HCID 137928 | — |
| Reactant | alpha-Nitro-beta-ethoxyacrylic acid methylester | HCID 53395203 | — |
| Product | Alpha-nitro-6-methyl-3-indoleacrylic acid methylester | HCID 54365062 | — |
Reaction Steps
A mixture of 32.5 g (0.25 mol) of 6-methylindole and 52.5 g (0.30 mol) of α-nitro-β-ethoxyacrylic acid methylester was let stand in a large crystallization dish at room temperature for 20 hours. The brown-orange solid was triturated with ether-hexane 1:1, the crystalline material collected by filtration, washed with ether and dried to afford 44.5 g. (69%) of product as orange crystals, m.p. 167°-169°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04256641 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-e1d95fc4561949359c3640c74721b0b7 |
| Source note | uspto-grants-1981_03 |