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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017640Generated: October 30, 2026

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

https://huagongshe.com/reaction/1017640

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 over 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 over MgSO4, filtered and concentrated in vacuo to give the desired acid (1.5 g, 87%). 1H NMR (300 MHz, DMSO) δ12.80, 7.96, 7.23-7.13, 7.04, 2.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479510B2
Source datasetuspto-grants-2002_11
ORD IDord-3ea3ae5b772b42569a3448cd5f1983cb
Source noteuspto-grants-2002_11