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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 5-methoxy-4-(3-bromopropoxy)-2-nitrobenzoateHCID 11727750—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 10149727HCID 10149727100%

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367824B2
Source datasetuspto-grants-2013_02
ORD IDord-091eaf64dd6c4631a8896404294bc937
Source noteuspto-grants-2013_02