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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197095Generated: November 1, 2026

Ethyl 4-nitro-2-[p-(4-phenylbutoxy)benzamido]phenoxyacetate → Ethyl 4-amino-2-[p-(4-phenylbutoxy)benzamido]phenoxyacetate

https://huagongshe.com/reaction/1197095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-nitro-2-[p-(4-phenylbutoxy)benzamido]phenoxyacetateHCID 15106476—
CatalystHCID 178418390HCID 178418390—
SolventTetrahydrofuran ethanolHCID 21873804—
ProductEthyl 4-amino-2-[p-(4-phenylbutoxy)benzamido]phenoxyacetateHCID 1510648165.2%

Reaction Steps

To a mixture of 2.81 g of ethyl 4-nitro-2-[p-(4-phenylbutoxy)benzamido]phenoxyacetate obtained in Example 26 in 50 ml of ethanol-tetrahydrofuran (1:1) was added 0.5 g of palladium-carbon. Catalytic reduction was performed at room temperature under normal pressure until absorption of hydrogen was discontinued. The catalyst was filtered off and the filtrate was concentrated under reduced pressure. The obtained crystals were washed with isopropyl alcohol to obtain 1.72 g of ethyl 4-amino-2-[p-(4-phenylbutoxy)benzamido]phenoxyacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116853
Source datasetuspto-grants-1992_05
ORD IDord-6f745e34fedf47d7822bd16ef75f170c
Source noteuspto-grants-1992_05