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HRID 348893作成日:2026年10月27日

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

https://huagongshe.com/reaction/348893

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Lithium borohydrideHCID 4148881—
反応物3-Bromo-5-(methoxycarbonyl)benzoic acidHCID 22593641—
反応物2,2-Dioxo-1,2,3,4-tetrahydro-2lambda6-benzo[c][1,2]thiazin-4-ylamineHCID 58802755—
溶媒EthanolHCID 702—
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US07176242B2
出典データセットuspto-grants-2007_02
ORD IDord-91d8f3927dd544c3b366b2775d57cab4
出典メモuspto-grants-2007_02