HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 4-Acetyl-2'-nitrobiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 2-Nitrobiphenyl | HCID 6829 | — |
| Reactant | 2-(2'-Nitro-4-biphenylyl)propionic acid | HCID 21453327 | — |
| Product | 4-Acetyl-2'-nitrobiphenyl | HCID 79805 | — |
Reaction Steps
The 2-(2'-nitro-4-biphenylyl)propionic acid is readily prepared in the following manner: 2-nitrobiphenyl is acylated with acetyl chloride, giving 4-acetyl-2'-nitrobiphenyl. This is converted with chloroacetonitrile under alkaline conditions to the intermediate isomeric 2-methyl-2-[4-(2'-nitrophenyl)]glycidonitriles which, when treated with lithium perchlorate and then base, is isomerized to methyl 2-(2'-nitro-4-biphenylyl)propionate. Saponificiation of the latter gives the desired 2-(2'-nitro-4-biphenylyl)propionic acid. The esters are readily converted to the acid and the acid to the esters by conventional means.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04009283 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-94c36a17fa604ec8a814ff9eca73baa3 |
| Source note | uspto-grants-1977_02 |