HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384804Generated: October 30, 2026
HCID 22466721, compound → HCID 22466729, compound
https://huagongshe.com/reaction/384804
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22466721 | HCID 22466721 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22466729 | HCID 22466729 | 102.1% |
Reaction Steps
In a 50 mL volume glass flask equipped with a stirrer, a thermometer, a reflux condenser and a gas inlet were placed 2.04 g (6.90 mmol) of 5-methoxy-4-(3-chloropropoxy)-2-nitrobenzoic acid (purity: 99%) obtained in Reference Example III-8 and 40 mL of methanol. The resulting mixture was heated to 40° C. under stirring. To the mixture was added 0.2 g of 5 wt. % palladium/carbon (containing 49% water) at the same temperature. The resulting mixture was heated to the same temperature for 2 hours, while hydrogen was introduced into the mixture under atmospheric pressure at a rate of 50 mL/min. After the reaction was complete, the reaction mixture was filtered and the filtrate was concentrated under reduced pressure, to precipitate a crystalline product. The crystalline product was dried under reduced pressure, to give 1.83 g (isolated yield: 97.0%, purity: 98% in terms of area percentage determined by high performance liquid chromatography) of 5-methoxy-4-(3-chloropropoxy)anthranilic acid as a white crystalline product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367824B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-a39d1c2b56ae45bab648cd9cd2460a5e |
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| Source note | uspto-grants-2013_02 |
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