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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384807Generated: October 30, 2026

Methyl 5-methoxy-4-(4-chlorobutoxy)-2-nitrobenzoate → HCID 10286203, compound

https://huagongshe.com/reaction/384807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-methoxy-4-(4-chlorobutoxy)-2-nitrobenzoateHCID 10215101—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 10286203HCID 10286203100%

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 (6.29 mmol) of methyl 5-methoxy-4-(4-chlorobutoxy)-2-nitrobenzoate (purity: 99%) obtained in Reference Example III-10, 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 1.81 g (isolated yield: 98.1%, purity: 98% in terms of area percentage determined by high performance liquid chromatography) of methyl 5-methoxy-4-(4-chlorobutoxy)anthranilate as a white crystalline product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367824B2
Source datasetuspto-grants-2013_02
ORD IDord-5dc51631af0f41e2bbb332209d810610
Source noteuspto-grants-2013_02