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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 650670Erstellt: 25. Oktober 2026

N-bromobutanimide → Methyl 5-(bromomethyl)thiophene-2-carboxylate

https://huagongshe.com/reaction/650670

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
EduktMethyl 5-methyl-2-thiophenecarboxylateHCID 580756—
EduktMethyl 5-(dibromomethyl)thiophene-2-carboxylateHCID 24179893—
LösungsmittelCarbon TetrachlorideHCID 5943—
ProduktMethyl 5-(bromomethyl)thiophene-2-carboxylateHCID 1142485125%

Reaktionsschritte

5-Methyl-thiophene-2-carboxylic acid methyl ester (20.0 g, 0.13 mol) was dissolved in a suspension of N-bromosuccinimide (45.4 g, 0.26 mol) and 2,2′-aza-bis-isobutyronitrile (0.1 g, 0.61 mmol) in 1 L of carbon tetrachloride. The suspension was refluxed for 48 hours then cooled and the precipitate was filtered off. The filtrate was concentrated and the residue was purified on silica gel (100% hexanes then 9:1 Hexanes-Ethyl acetate) to provide a 26 g fraction containing mainly the di-brominated compound 5-dibromomethyl-thiophene-2-carboxylic acid methyl ester as a yellow oil and a more polar fraction (7.5 g) containing mainly compound T-1 (25% yield) as a yellow oil (70% purity).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06274620B1
Quelldatensatzuspto-grants-2001_08
ORD IDord-b123d0dea85948b8834e85b7e638c417
Quellennotizuspto-grants-2001_08