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HRID 11068Erstellt: 24. Oktober 2026

Bromide ion → (2,6-Dibromobenzyl)(triphenyl)phosphonium bromide

https://huagongshe.com/de/reaction/11068

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromide ionHCID 259—
EduktTriphenylphosphineHCID 11776—
Edukt2,6-DibromotolueneHCID 34681—
EduktNbs aibnHCID 86630000—
LösungsmittelMethane, dichloro-, compd. with benzene (1:1)HCID 23443464—
Produkt(2,6-Dibromobenzyl)(triphenyl)phosphonium bromideHCID 8789908995%

Reaktionsschritte

Bromination of 2,6-dibromotoluene with NBS/AIBN, followed by reaction of the crude bromide with triphenylphosphine, using the procedure described in example 102, except that the reaction time for the bromination was 3 h, gave the phosphonium salt (516) (95%) as a cream powder, mp (CH2Cl2/benzene) 241–243° C. 1H NMR (CDCl3) δ 7.78 (m, 9H), 7.64 (m, 6H), 7.40 (br d, J=7.9 Hz, 2H), 6.99 (td, J=8.0, 2.5 Hz, 1H), 5.58 (d, J=14.1 Hz, 2H). Found: C, 47.06; H, 3.37. C25H20Br3P.3/4 CH2Cl2 requires C, 47.23; H, 3.31.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094798B1
Quelldatensatzuspto-grants-2006_08
ORD IDord-62d61bd7e7f844569eafefc807ca8df6
Quellennotizuspto-grants-2006_08