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HRID 322949作成日:2026年10月25日

Potassium Hydroxide → 2-Nitro-5-(3-thienylmethoxy)phenol

https://huagongshe.com/reaction/322949

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物2-Fluoro-4-(3-thienylmethoxy)nitrobenzeneHCID 22010146—
溶媒tert-ButanolHCID 6386—
生成物2-Nitro-5-(3-thienylmethoxy)phenolHCID 22010342—

反応手順

A mixture of 2-fluoro-4-(3-thienylmethoxy)nitrobenzene (4.21 g), aqueous potassium hydroxide solution (50 mL; 50% w/v) and t-butanol (20 mL) is heated at reflux for 4 hours. It is then evaporated to dryness and the residue is partitioned between ethyl acetate (100 mL) and hydrochloric acid (100 mL; 1 N). The organic phase is washed with water (3×100 mL), dried over magnesium sulphate, filtered and evaporated, to give 2-nitro-5-(3-thienylmethoxy)phenol, in the form of a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211234B1
出典データセットuspto-grants-2001_04
ORD IDord-90c13fef15b74e0bbc01c05a818beff2
出典メモuspto-grants-2001_04