HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384801Generated: October 30, 2026
methyl 5-methoxy-4-(3-bromopropoxy)-2-nitrobenzoate → HCID 10149727, compound
https://huagongshe.com/reaction/384801
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | methyl 5-methoxy-4-(3-bromopropoxy)-2-nitrobenzoate | HCID 11727750 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10149727 | HCID 10149727 | 100% |
Reaction Steps
In a 50 mL volume glass flask equipped with a stirrer, a thermometer, a reflux condenser and a gas inlet were placed 2.02 g (5.75 mmol) of methyl 5-methoxy-4-(3-bromopropoxy)-2-nitrobenzoate (purity: 99%) obtained in Reference Example III-6 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). The resulting mixture was heated to the same temperature for 2 hours, while hydrogen was introduced to the mixture under atmospheric pressure at a rate of 50 mL/min. After the reaction was complete, the reaction mixture was filtered. The filtrate was concentrated under reduced pressure, precipitating a crystalline product. The crystalline product was dried under reduce pressure, to give 1.83 g (isolated yield: 98.1%, purity: 98% in terms of area percentage determined by high performance liquid chromatography) of methyl 5-methoxy-4-(3-bromopropoxy)anthranilate.
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-091eaf64dd6c4631a8896404294bc937 |
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| Source note | uspto-grants-2013_02 |
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