HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxy-3,5-dinitrobenzaldehyde → HCID 22763893, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxy-3,5-dinitrobenzaldehyde | HCID 104091 | — |
| Reactant | HCID 22763917 | HCID 22763917 | — |
| Reactant | HCID 178526649 | HCID 178526649 | — |
| Product | HCID 22763893 | HCID 22763893 | — |
Reaction Steps
Compounds in which the substituent in the 6(5) position of the benzene ring of the benzimidazole is difluoromethyl are prepared from 2,6-dinitro-4-difluoromethylbenzene according to the above procedure. This latter compound is prepared by the reaction of SF4 and 3,5-dinitro-4-hydroxybenzaldehyde to yield 2,6-dinitro-4-difluoromethylphenol which is converted to the corresponding chloride by conventional means. 2-Trifluoromethyl-4-nitro-6-difluoromethylbenzimidazole was prepared from the above diamine by the process of the above example and melted at about 132°-134° C. after recrystallization from benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04122184 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-71a54c7f266a4bdca8fd9ba0c68a4e60 |
| Source note | uspto-grants-1978_10 |