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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655023Generated: November 1, 2026

Ethyl Acetate → 7-Hydroxycarbostyril

https://huagongshe.com/reaction/1655023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3-AminophenolHCID 11568—
Reactant3-Phenylprop-2-enoyl chlorideHCID 66023—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product7-HydroxycarbostyrilHCID 10975787—

Reaction Steps

To a solution of 3-aminophenol (1 g) in CH2Cl2 (25 mL) and pyridine (1 mL) at 5° C. was added dropwise a solution of cinnamoyl chloride (1.53 g) in CH2Cl2 (10 mL). The mixture was warmed to r.t. over 1 hr, and then EtOAc (150 mL) was added. The organics were washed with H2O, 1N, HCl, saturated aq. NaHCO3 and H2O, dried (MgSO4) and concentrated. To the residue was added AlCl3 (6.38 g) and the mixture heated at 180° C. for 5 min. and then at 115°-120° C. for 2 hr. To the mixture was added ice and then H2O. The solid that formed was collected by filtration, washed with 2N HCl and H2O (3×). The resulting solid was triturated in EtOAc to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05410054
Source datasetuspto-grants-1995_04
ORD IDord-84bcab8d5fb54118a5f5807ebd975af0
Source noteuspto-grants-1995_04