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HRID 129594作成日:2026年10月26日

3-Hydroxybenzyl alcohol → 2-(3-Hydroxymethylphenoxy)phenylacetic acid

https://huagongshe.com/reaction/129594

反応式

関与物質

役割名称HCID仕込み量
反応物3-Hydroxybenzyl alcoholHCID 102—
反応物Hydrochloric AcidHCID 313—
反応物Potassium CarbonateHCID 11430—
反応物2-Bromophenylacetic acidHCID 87754—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-(3-Hydroxymethylphenoxy)phenylacetic acidHCID 15125737130.1%

反応条件

温度140 °C

反応手順

3-Hydroxybenzyl alcohol (31.0 g) was ground finely and stirred with potassium carbonate (34.6 g), 2-bromophenylacetic acid (26.9 g) and cuprous chloride (large spatula full) under nitrogen. The mixture was warmed to 140° C., and stirred vigorously for 31/2 hours. DMF (60 ml) was then added to the stirred melt and the solution was allowed to cool, poured into water and acidified with dilute hydrochloric acid. The aqueous layer was extracted with ether, and the ether extracts were washed with water, dried and evaporated to give 2-(3-hydroxymethylphenoxy)phenylacetic acid as a brown oil (42.03 g) which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05468857
出典データセットuspto-grants-1995_11
ORD IDord-ccde36f6580d4ba39e2922e675ab5822
出典メモuspto-grants-1995_11