HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534857Generated: November 2, 2026
Methyl Anthranilate → HCID 15084048, compound
https://huagongshe.com/reaction/1534857
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Anthranilate | HCID 8635 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 15084048 | HCID 15084048 | 74.2% |
Reaction Steps
To a suspension of 12.6 g (100 mmol) of the sodium salt obtained in the above (i) in 100 ml of benzene was dropwise added 8.0 ml (110 mmol) of thionyl chloride under stirring at room temperature for a period of 5 min. The mixture was then heated under reflux for 30 min. After chilling with ice, insolubles were removed by filtration. To the filtrate were added 15.1 g (100 mmol) of methyl anthranilate and 13.8 g (100 mmol) of potassium carbonate. The resulting mixture was then heated under reflux for 4 hrs. After the addition of ice water, the reaction mixture was washed sequentially with 6 N hydrochloric acid, saturated aqueous sodium hydrogencarbonate and saturated aqueous sodium chloride, and then was dried over anhydrous sodium sulfate. The solvent was distilled off to leave 8.8 g of an oily product. The oily product was crystallized from hexane to give 8.3 g of the desired compound as a pale yellow crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05091403 |
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| Source dataset | uspto-grants-1992_02 |
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| ORD ID | ord-faa94a97d1024c43a5985d926f5a40d8 |
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| Source note | uspto-grants-1992_02 |
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