戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1660804作成日:2026年10月26日

Hydrochloric Acid → 4-(Benzyloxy)-3-nitrobenzoic acid

https://huagongshe.com/reaction/1660804

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物MethanolHCID 887—
反応物Potassium HydroxideHCID 14797—
反応物Methyl 4-benzyloxy-3-nitrobenzoateHCID 289857—
溶媒TetrahydrofuranHCID 8028—
生成物4-(Benzyloxy)-3-nitrobenzoic acidHCID 1612472595%

反応手順

A solution the crude 4-benzyloxy-3-nitro-benzoic acid methyl ester from the previous step in tetrahydrofurane (150 mL) and MeOH (600 mL) was treated with KOH 3N (152 mL) and stirred at room temperature for 18 hours. The mixture was acidified with HCl 3N. The precipitate thus formed was filtered, washing with MeOH/water 1:1 and dried under vacuum. 4-Benzyloxy-3-nitro-benzoic acid (42 g, 95% over two steps) was obtained as a white solid, which was used crude in the following reaction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08030308B2
出典データセットuspto-grants-2011_10
ORD IDord-6161a1f249a54a6e83476b70aa6fb3b5
出典メモuspto-grants-2011_10