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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20698Erstellt: 24. Oktober 2026

Benzene, ((2-bromoethoxy)methyl)- → Ethyl 4-(benzyloxy)-2-(2,3-bis(cyclopentyloxy)-4-methoxybenzoyl)butanoate

https://huagongshe.com/de/reaction/20698

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzene, ((2-bromoethoxy)methyl)-HCID 73833—
EduktSodium ethoxideHCID 2723922—
EduktMethyl 3-(2,3-bis(cyclopentyloxy)-4-methoxyphenyl)-3-oxopropanoateHCID 68742690—
LösungsmittelEthanolHCID 702—
ProduktEthyl 4-(benzyloxy)-2-(2,3-bis(cyclopentyloxy)-4-methoxybenzoyl)butanoateHCID 68741697—

Reaktionsschritte

Sodium ethoxide (2.0 g, 29 mmol) was added to a solution of methyl 3-(2,3-bis(cyclopentyloxy)-4-methoxyphenyl)-3-oxopropanoate (11 g, 29 mmol) and ethanol (150 mL) at rt. After refluxing for 1 h, ((2-bromoethoxy)methyl)benzene (12.5 g, 57.8 mmol) was added and refluxing was continued overnight. The reaction was allowed to cool to rt, concentrated, diluted with ethyl acetate (300 mL), and then washed with brine (50 mL×2). The organic layer was dried, filtered, concentrated, and purified by silica gel chromatography (ethyl acetate:petroleum ether) to give ethyl 4-(benzyloxy)-2-(2,3-bis(cyclopentyloxy)-4-methoxybenzoyl)butanoate: MS (ESI): 525.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745646B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-b5572fcb9d9044329d31676381ddbca5
Quellennotizuspto-grants-2010_06