HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-(methylsulfonamido)-5-nitrobenzoate → Methyl 3-amino-5-(methylsulfonamido)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-(methylsulfonamido)-5-nitrobenzoate | HCID 57815097 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-amino-5-(methylsulfonamido)benzoate | HCID 59243082 | — |
Reaction Steps
3-methylsulfonylamino-5-nitro-benzoic acid methyl ester (32 g; 0.12 mol) was suspended in methanol (500 ml), 4 g (5% w/w; 4 g) was added and the mixture was hydrogenated at 4-5 bar. The reaction mixture was subsequently filtered on a Celite pad and the filtrate concentrated. 23 g (0.08 mmol; 66% yield) of a yellow powder were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410100B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-56b4fd4c9bb94bc69ffff4626f363f5f |
| Source note | uspto-grants-2013_04 |