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HRID 1605635作成日:2026年10月27日

Butyric Acid → 4-Methoxyphenol

https://huagongshe.com/reaction/1605635

反応式

関与物質

役割名称HCID仕込み量
反応物Butyric AcidHCID 264—
反応物GuaiacolHCID 460—
反応物AnisoleHCID 7519—
反応物Perpropionic acidHCID 65136—
反応物Dimethyl phosphate anionHCID 3753418—
反応物Methyl PhosphateHCID 12691389—
生成物4-MethoxyphenolHCID 9015—

反応条件

温度80 °C

反応手順

The procedure of Example 23 was repeated, except 1 mol of anisole was used in place of phenol. To the solution in the flask, 0.2g of a mixture of dimethyl phosphate and monomethyl phosphate (available on the market under the designation of "dimethyl phosphate" and containing about 50 percent of dimethyl phosphate, the remainder being monomethyl phosphate) was added and heated to 80°C. Then 0.1 of perpropionic acid (prepared in the form of 30 percent ethyl acetic acid solution) was introduced dropwise over a period of about 20 minutes. At the end of three hours following the start of said dropwise introduction of acid solution, the reaction solution was analyzed by repeating the procedure of Example 23. The analysis showed that 2.85g of pyrocatechol monomethyl ether and 1.44g of hydroquinone monomethyl ether were produced, with the conversion of perpropionic acid at 99.1 percent and that of anisole at 6.0 percent. When this reaction was performed in the absence of the catalyst, the yield of pyrocatechol monomethyl ether was 2.01g and that of hydroquinone monomethyl ether was 1.00g, although the conversion of each of the reactants was substantially the same.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03950437
出典データセットuspto-grants-1976_04
ORD IDord-49612dd44a5f431eb3ef90d5dad17123
出典メモuspto-grants-1976_04