alpha-ethoxy-p-cresol
alpha-ethoxy-p-cresol Basic information
- Product Name:
- alpha-ethoxy-p-cresol
- Synonyms:
-
- alpha-ethoxy-p-cresol
- Phenol, 4-(ethoxymethyl)-
- 4-(Ethoxymethyl)phenol
- 4-Ethoxymethylphenol
- alpha-Ethoxy-p-creso
- p-Hydroxybenzyl ethyl ether
- 4-hydroxybenzyl ethyl ether
- p-Hydroxybenzyl Et ether
- CAS:
- 57726-26-8
- MF:
- C9H12O2
- MW:
- 152.19
- EINECS:
- 260-918-4
- Mol File:
- 57726-26-8.mol
alpha-ethoxy-p-cresol Chemical Properties
- storage temp.
- Inert atmosphere,Room Temperature
- form
- Solid
- color
- White to off-white
- LogP
- 1.699 (est)
alpha-ethoxy-p-cresol Usage And Synthesis
Uses
4-(Ethoxymethyl)phenol (p-Hydroxybenzyl Et ether) is a potent antioxidant from Amburana cearensis leaf extract, with in vitro cytogenotoxic properties. Amburana cearensis leaves can be used foe the research of respiratory diseases and inflammations[1].
Definition
ChEBI: 4-(Ethoxymethyl)phenol is a benzyl ether.
Synthesis
64-17-5
623-05-2
57726-26-8
General procedure for the synthesis of 4-(ethoxymethyl)phenol from ethanol and p-hydroxybenzyl alcohol: refer to the operation of Example 2, but substitute ethanol for methanol. After completion of the reaction, the residue was purified by reduced pressure distillation (boiling point: 110-119°C/1.5 Torr) to obtain 4-ethoxymethylphenol in 75% yield and 98% HPLC purity. The operation was as follows: in a 200 mL three-necked flask equipped with a thermometer, a three-way stopper and a stirrer, 15.0 g (0.12 mol) of p-hydroxybenzyl alcohol and 69 g of ethanol were added under nitrogen protection, followed by 0.06 g of nitromethane. A mixed solution consisting of 0.45 g of hydrochloric acid and 3.0 g of ethanol was slowly added dropwise under stirring at room temperature, and then the reaction mixture was stirred at 35 °C for 3 hours. At the end of the reaction, HPLC analysis showed an area percentage of 99%. Next, a mixed solution comprising 0.38 g of imidazole (manufactured by Aldrich Co., Ltd.) and 1.1 g of ethanol was added dropwise for neutralization, followed by concentration under reduced pressure to remove ethanol. To the concentrate, 60 g of isopropyl ether (produced by Nacalai Tesque, Inc.) and 22.5 g of water were added and the organic layer was further washed with 27 g of water and 0.26 g of acetic acid (produced by Nacalai Tesque). After washing the organic layer twice with water, the organic layer was concentrated, the crystal seed was added and slowly cooled to about 8°C. The precipitated crystals were filtered and dried to give 12.0 g (yield: 72%) of colorless 4-methoxymethylphenol with 99% HPLC purity.
References
[1] José Rafael da Silva Araujo, et al. Antioxidant and in vitro cytogenotoxic properties of Amburana cearensis (Allem?o) A.C.Sm. leaf extract. Drug Chem Toxicol. 2021 Dec 14;1-9. DOI:10.1080/01480545.2021.2011313
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