HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-Amino-6-nitro-benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium hydrosulfide | HCID 28015 | — |
| Reactant | Benzoic acid, 2,6-dinitro- | HCID 119206 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-6-nitro-benzoic acid | HCID 95795 | — |
Reaction Steps
In one non-limiting reaction scheme, dinitrobenzoic acid may be reacted with about one to about five equivalents of an alkali hydrosulfide in a methanol:water mixture at reflux temperature for about 20 to about 40 minutes to produce an aminonitrobenzoic acid. As is described in the Example below, 2,6-dinitrobenzoic acid may be allowed to react with about three equivalents of sodium hydrosulfide in a methanol:water mixture at reflux temperature for about 30 minutes to produce 2-amino-6-nitrobenzoic acid. In some non-limiting embodiments, three equivalents of sodium hydrosulfide may be reacted with one equivalent of the sodium salt of 2,6-dinitrobenzoic acid in refluxing methanol/water followed by acidification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08835677B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-69bad618805b4b82beaba1d05b555cee |
| Source note | uspto-grants-2014_09 |