HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorine → N'-tert-butylbenzohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | HCID 2797474 | HCID 2797474 | — |
| Reactant | HCID 15617772 | HCID 15617772 | — |
| Reactant | HCID 15617773 | HCID 15617773 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | N'-tert-butylbenzohydrazide | HCID 299436 | — |
Reaction Steps
The above reactions are illustrated below: ##STR15## wherein Q is halogen, preferably chlorine; R is tert-butyl or tert-amyl. Other compounds that can be prepared by the above procedure using the appropriately substituted benzoyl halide include: m-chlorobenzoic acid, 2-tert-butylhydrazide, mp 120°-123° C.; p-cyanobenzoic acid, 2-tert-butylhydrazide, mp 135°-136° C.; anthranilic acid, 2-tert-butylhydrazide, mp 165°-167° C.; tert-butyl or isopropyl; and X is hydrogen, halogen, C1 -C3 alkyl, methoxy, methylamino, NH2, nitro or CF3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04814349 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-82b9742e4069431e9733b8dc104bf970 |
| Source note | uspto-grants-1989_03 |