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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 521484Erstellt: 26. Oktober 2026

3-Bromo-4-methoxybenzoic acid → 2-(3-Bromo-4-methoxy-benzoylamino)-indane-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/521484

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Bromo-4-methoxybenzoic acidHCID 66836—
Eduktmethyl 2-amino-2,3-dihydro-1H-indene-2-carboxylate hydrochlorideHCID 45074056—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelThionyl ChlorideHCID 24386—
Produkt2-(3-Bromo-4-methoxy-benzoylamino)-indane-2-carboxylic acid methyl esterHCID 6707633081,8%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

3-Bromo-4-methoxybenzoic acid (22.8 g, 98.8 mmol) was dissolved in thionyl chloride (42 ml) and stirred at 60° C. for 30 min. The volatiles were evaporated in vacuo and the residue was stripped with dioxane. The obtained acid chloride was dissolved in DCM (50 ml). 2-Amino-indane-2-carboxylic acid methyl ester hydrochloride (15.0 g, 65.9 mmol) was suspended in DCM (100 ml), EDIA (10.2 g, 79.1 mmol) was added, the mixture was cooled in an ice bath, and the solution of the acid chloride was slowly added. The mixture was stirred overnight at room temperature and evaporated to dryness. The residue was purified by silica gel chromatography (DCM/methanol gradient) and subsequent crystallization from EA to give 21.8 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09328071B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-30e0985f63e94214b75c8d1c2a4714ff
Quellennotizuspto-grants-2016_05