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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 4-(4-Hydroxy-phenoxy)-benzoic acid | HCID 615542 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Acetoxyphenoxy)benzoic acid | HCID 22573465 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479510B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-3ea3ae5b772b42569a3448cd5f1983cb |
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| Source note | uspto-grants-2002_11 |
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