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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393278Generated: October 31, 2026

Ethyl 5-(4-Aminophenyl)-2-Methyl-3-Furoate → Ethyl 5-(4-hydroxyphenyl)-2-methyl-3-furanecarboxylate

https://huagongshe.com/reaction/393278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-(4-Aminophenyl)-2-Methyl-3-FuroateHCID 2742184—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
ProductEthyl 5-(4-hydroxyphenyl)-2-methyl-3-furanecarboxylateHCID 2264885920%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of NaNO2 (111 mg, 1.61 mmol) in water (1 mL) was added over 5 min to an ice-cold suspension of ethyl 5-(4-aminophenyl)-2-methyl-3-furanecarboxylate (395 mg, 1.61 mmol) in aqueous 1 M H2SO4 solution (12 mL). The reaction mixture was stirred at 0° C. for 20 min then was heated to 90° C. for 1 h. The cooled mixture was extracted with EtOAc. The organic layer was washed with water (2×) and brine, dried (MgSO4), filtered and concentrated under reduced pressure to yield the title compound (78 mg, 20% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806265B2
Source datasetuspto-grants-2004_10
ORD IDord-371b50119d0c4c279cf533262f1fe6ab
Source noteuspto-grants-2004_10