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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 842734Erstellt: 25. Oktober 2026

Methyl 5-bromothiophene-2-carboxylate → 5-(3-tert-Butoxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic Acid Methyl Ester

https://huagongshe.com/reaction/842734

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 5-bromothiophene-2-carboxylateHCID 605713—
Edukttert-butyl N-(prop-2-yn-1-yl)carbamateHCID 11073648—
KatalysatorTriethylamineHCID 8471—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-(3-tert-Butoxycarbonylamino-prop-1-ynyl)-thiophene-2-carboxylic Acid Methyl EsterHCID 5407533963.406,199%

Reaktionsschritte

A mixture of prop-2-ynyl-carbamic acid tert-butyl ester (1.67 g, 0.011 mmol), 5-bromo-thiophene-2-carboxylic acid methyl ester (2.50 g, 0.011 mmol), tetrakistriphenylphosphine(0) palladium (0.622 9, 0.0538 mmol), Cul (0.102 g, 0.538 mmol) and triethylamine (1.57 mL, 0.011 mmol) in 50 mL acetonitrile was heated at reflux for 16 h. The reaction was cooled to room temperature, diluted with 75 mL EtOAc, washed with 5.5% HCl, water and brine, dried over MgSO4, filtered and concentrated in vacuo to an oil. The product was purified via flash chromatography (9:1 to 4:1 hexanes:EtOAc) to afford the title compound as an oil (2.06 g). MS 313 (M+18).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06376502B1
Quelldatensatzuspto-grants-2002_04
ORD IDord-73c16622ab3c4a548911a8e84df0f09f
Quellennotizuspto-grants-2002_04