HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-5-methyl-3-nitropyridine → 2-[4-Cyano-1,1-dicarbethoxybutyl]-3-nitro-5-methylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-5-methyl-3-nitropyridine | HCID 818300 | — |
| Reactant | Diethyl 2-(3-cyanopropyl)malonate | HCID 3641060 | — |
| Product | 2-[4-Cyano-1,1-dicarbethoxybutyl]-3-nitro-5-methylpyridine | HCID 20271457 | — |
Reaction Steps
2-Chloro-5-methyl-3-nitro-pyridine (20 g) was reacted with 2-(3-cyanopropyl)malonic acid diethyl ester under conditions analogous to those in Example 1(a). The reaction mixture was partitioned between water and chloroform, the chloroform extract was dried, treated with charcoal and filtered through a silica bed and then evaporated to a dryness to give 2-[4-cyano-1,1-dicarbethoxybutyl]-3-nitro-5-methylpyridine (18.3 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04535163 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-c0912b86b312495cbe4010e2b572e24e |
| Source note | uspto-grants-1985_08 |