Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23373Generated: October 30, 2026

Acetyl chloride → 4-(4-Acetoxyphenoxy)benzoic acid

https://huagongshe.com/reaction/23373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant4-(4-Hydroxy-phenoxy)-benzoic acidHCID 615542—
SolventDichloromethaneHCID 6344—
Product4-(4-Acetoxyphenoxy)benzoic acidHCID 2257346587%

Reaction Steps

Acetylchloride (1.5 mL, 21 mmol) is added to a solution of 4-(4-hydroxyphenoxy)benzoic acid (2.3 g, 10 mmol) and TEA (2.9 mL, 21 mmol) in CH2Cl2 (50 mL). The reaction is stirred for 16 hours at room temperature. The reaction mixture is diluted with CH2Cl2 and washed three times with saturated NaHCO3. The organic layer is dried (MgSO4), filtered and concentrated in vacuo. The resulting material is dissolved in dioxane (6 mL). Aqueous LiOH (1N, 930 μL) is added, and the reaction is allowed to stir for one hour at room temperature. The reaction mixture is poured into CH2Cl2 and washed twice with KHSO4. The organic layer is dried (MgSO4), filtered and concentrated in vacuo to give 4-(4-acetoxyphenoxy)benzoic acid (1.5 g, 87%). 1H NMR (300 MHz, DMSO) δ 12.80, 7.96, 7.23-7.13, 7.04, 2.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852716B2
Source datasetuspto-grants-2005_02
ORD IDord-57713b86a77642e28b6eb5f0508e6d42
Source noteuspto-grants-2005_02