HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 2-Amino-5-chlorobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 21584726 | HCID 21584726 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Amino-5-chlorobenzoic acid | HCID 12476 | 59% |
Reaction Steps
1.0 g (5.1 mmol) of 5-chloroisatoic acid was heated under stirring in a mixed solvent of benzyl alcohol (5 mL) and DMF (5 mL) at 100° C. for 5 hours. After cooling, the reaction mixture was diluted with ethyl acetate, and washed with water. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The resulting crude product was separated and purified using silica gel column chromatography to give 0.516 g of 2-amino-5-chlorobenzoic acid.benzylester (yield: 39%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08415479B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-ee74b51925a94b6abad65c37346639ab |
| Source note | uspto-grants-2013_04 |