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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591039Generated: October 30, 2026

Tetrahydrofuran → HCID 19766031, compound

https://huagongshe.com/reaction/1591039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantSodium HydroxideHCID 14798—
Reactant4-Aminobenzene-1,3-diol hydrochlorideHCID 13408822—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 19766031HCID 1976603127.2%

Reaction Steps

25 g (142.8 mmol) of 4-chlorobenzoyl chloride and 3.0 g (18.6 mmol) of 4-aminoresorcinol hydrochloride were introduced into a three-necked flask provided with a thermometer and a cooling condenser, and the mixture was heated at 170° to 200° C. for 1 hour, then the excessive acid chloride was removed by distillation. To the residue, 8.4 g (210 mmol) of NaOH, 60 ml of THF, 60 ml of water and 30 ml of methanol were added, and the mixture was stirred at room temperature for about 2 hours. The reaction solution was extracted with ethyl acetate, the extract was washed with saturated sodium chloride water solution, and ethyl acetate was distilled off. Recrystallizing the residue with water/methanol/THF and drying the crystal, there was obtained 1.24 g (5.05 mmol) of 2-(4-chlorophenyl)-6-hydroxybenzoxazole. The yield was 27.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05206149
Source datasetuspto-grants-1993_04
ORD IDord-84d0e2a7cc26477a95aa49f044373af8
Source noteuspto-grants-1993_04