HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Methyl 5-amino-2-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Amino-2-nitrobenzoic acid | HCID 83298 | — |
| Reactant | 2-Amino-5-piperidin-1-yl-benzoic acid ethyl ester | HCID 61306567 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 5-amino-2-nitrobenzoate | HCID 11446896 | 42% |
Reaction Steps
5-Amino-2-nitro-benzoic acid (compound A′) (910 mg) was dissolved in methanol (50 ml). Thionyl chloride (0.74 ml) was added dropwise to the solution on an ice bath, and a reaction was allowed to proceed under reflux with heating for 12 hr. After the completion of the reaction, the reaction solution was allowed to stand for cooling to room temperature and was then concentrated under the reduced pressure. The residue was purified by column chromatography eluted with a chloroform-methanol system to give 5-amino-2-nitro-benzoic acid methyl ester (410 mg, yield 42%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08134015B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-4bd5328ed55747c48fbafa16bc0bea07 |
| Source note | uspto-grants-2012_03 |