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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11148Erstellt: 24. Oktober 2026

Bromide ion → (2-Methoxy-4-nitrobenzyl)(triphenyl)phosphonium bromide

https://huagongshe.com/de/reaction/11148

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromide ionHCID 259—
EduktHydrogen BromideHCID 260—
EduktTriphenylphosphineHCID 11776—
Edukt2-Methoxy-4-nitrobenzyl alcoholHCID 10487701—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethane, dichloro-, compd. with benzene (1:1)HCID 23443464—
Produkt(2-Methoxy-4-nitrobenzyl)(triphenyl)phosphonium bromideHCID 8789896884%

Reaktionsschritte

Bromination of (2-methoxy-4-nitrophenyl)methanol with 30% HBr in acetic acid, followed by reaction of the crude bromide with triphenylphosphine, using the procedure described in example 112, except that the conditions for the displacement were 3 days at 20° C. followed by 1 day at 55° C., gave the phosphonium salt (582) (84%) as a yellow solid, mp (CH2Cl2/benzene) 194–196° C. 1H NMR (CDCl3) δ 7.83–7.63 (m, 17H), 7.45 (br s, 1H), 5.52 (d, J=15.0 Hz, 2H). Found: C, 61.10; H, 4.73; N, 3.05. C26H23BrNO3P requires C, 61.43; H, 4.56; N, 2.76.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094798B1
Quelldatensatzuspto-grants-2006_08
ORD IDord-9d994210277644129c424413fa4c52d0
Quellennotizuspto-grants-2006_08