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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1816725Erstellt: 26. Oktober 2026

Water → 5-Bromo-2-(7-bromoheptyloxy)-1,3-dimethylbenzene

https://huagongshe.com/reaction/1816725

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
Edukt4-Bromo-2,6-dimethylphenolHCID 16919—
Edukt1,7-DibromoheptaneHCID 78309—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-Bromo-2-(7-bromoheptyloxy)-1,3-dimethylbenzeneHCID 22494636—

Reaktionsschritte

A solution of 4-bromo-2,6-dimethylphenol (2.00 g) and 1,7-dibromoheptane (5.10 g) in N,N-dimethylformamide (20 ml) was treated with potassium carbonate (2.06 g), and the mixture was stirred for 5 hours at ambient temperature. To the reaction mixture was added water and methylene chloride, and the organic layer was separated and dried over magnesium sulfate. Magnesium sulfate was filtered off, and the filtrate was concentrated in vacuo. The residue was purified by silica gel column chromatography eluting successively with the following solvents: (1) n-hexane, (2) n-hexane:ethyl acetate=4:1, (3) n-hexane:ethyl acetate=1:1. The fractions containing the object compound were concentrated in vacuo to give crude 5-bromo-2-(7-bromoheptyloxy)-1,3-dimethylbenzene, that was used in the next reaction directly, as a pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06884868B1
Quelldatensatzuspto-grants-2005_04
ORD IDord-7fc2b0d85ff048f1a19a243b72b12415
Quellennotizuspto-grants-2005_04