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HRID 14101作成日:2026年10月24日

Hydrochloric Acid → 3-Bromo-5-(hydroxymethyl)benzoic acid

https://huagongshe.com/ja/reaction/14101

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EthanolHCID 702—
反応物Lithium borohydrideHCID 4148881—
反応物3-Bromo-5-(methoxycarbonyl)benzoic acidHCID 22593641—
溶媒TetrahydrofuranHCID 8028—
生成物3-Bromo-5-(hydroxymethyl)benzoic acidHCID 8167127—

反応手順

To an ice-cold solution of 3-bromo-5-(methoxycarbonyl)benzoic acid prepared by the method in Preparation 2 (10.3 g, 40 mmol) in anhydrous tetrahydrofuran (100 mL) is added lithium borohydride (12 g, 550 mmol) portion-wise. The reaction is stirred 4 h at this temperature. Absolute ethanol (20 mL) is added dropwise, and the reaction is stirred 1.5 h. The reaction is slowly poured on ice, and 10% hydrochloric acid (aq) is added until gas evolution ceased. The aqueous layer is extracted with chloroform, and the organic layer is washed with brine, dried (magnesium sulfate), filtered, and concentrated under reduced pressure to give the title compound. ESI MS m/z 229, 231 [M−H]−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727997B2
出典データセットuspto-grants-2010_06
ORD IDord-479f562303ec43e8b64ace9bb92a85a5
出典メモuspto-grants-2010_06