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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 348893Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/348893

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktLithium borohydrideHCID 4148881—
Edukt3-Bromo-5-(methoxycarbonyl)benzoic acidHCID 22593641—
Edukt2,2-Dioxo-1,2,3,4-tetrahydro-2lambda6-benzo[c][1,2]thiazin-4-ylamineHCID 58802755—
LösungsmittelEthanolHCID 702—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Bromo-5-(hydroxymethyl)benzoic acidHCID 8167127—

Reaktionsschritte

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]−.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07176242B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-91d8f3927dd544c3b366b2775d57cab4
Quellennotizuspto-grants-2007_02