HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299207Generated: October 30, 2026
Sodium Bicarbonate → HCID 21958042, compound
https://huagongshe.com/reaction/2299207
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 4-Amino-3-chlorobenzoate | HCID 1515284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Benzyl chloroformate | HCID 10387 | — |
| Product | HCID 21958042 | HCID 21958042 | 154.3% |
Reaction Steps
Methyl 4-amino-3-chlorobenzoate (5.65 g; synthesized in accordance with Synthesis, 1985, 669) was dissolved in tetrahydrofuran (112 ml) and admixed with a solution of sodium hydrogen carbonate (7.67 g) in water (84.8 ml) and benzyl chloroformate (39.1 ml) and the mixture was stirred under a nitrogen atmosphere at room temperature for 22.5 hours. The reaction mixture was extracted with ethyl acetate and the ethyl acetate layer was washed three times with water and then twice with saturated brine. The ethyl acetate layer was dried over magnesium sulfate and then the solvent was distilled off under reduced pressure, and then the residue was purified by column chromatography on silica gel (ethyl acetate/hexane=1:7). A desired fraction was concentrated under reduced pressure and the residue was crystallized from a mixture of ethyl acetate and diisopropyl ether to yield methyl 4-benzyloxycarbonylamino-3-chlorobenzoate (7.51 g) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06495604B1 |
|---|
| Source dataset | uspto-grants-2002_12 |
|---|
| ORD ID | ord-98d70507884145358f79f5a95c49ed87 |
|---|
| Source note | uspto-grants-2002_12 |
|---|