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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 416418Erstellt: 25. Oktober 2026

Carbon tetrabromide → Di-tert-butyl phosphorobromidate

https://huagongshe.com/reaction/416418

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon tetrabromideHCID 11205—
EduktSodium HydroxideHCID 14798—
EduktPhosphiteHCID 107908—
EduktDi-tert-butyl phosphiteHCID 21959072—
KatalysatorBenzyl triethylammonium chlorideHCID 66133—
LösungsmittelDichloromethaneHCID 6344—
ProduktDi-tert-butyl phosphorobromidateHCID 10934607172,1%

Reaktionsschritte

A 500 mL 3-neck flask equipped with dropping funnel and thermometer was charged with carbon tetrabromide (16.58 g, 50 mmol), benzyltriethylammonium chloride (1.14 g, 5.0 mmol) and dichloromethane (50 mL). A 20% w/w NaOH solution (50 mL) was added with vigorous stirring, followed by dropwise addition of a solution of di-tert-butylphosphite (20 g, 100 mmol) in dichloromethane (20 mL), the rate of addition was controlled to keep the temperature of reaction mixture not to exceed to 25° C. After addition of phosphite, the mixture was further stirred at room temperature for 3 h, diluted with dichloromethane (20 mL) and separated. The organic phase was washed with saturated sodium bisulfite, water, brine, dried (Na2SO4), filtered and concentrated at RT. After removing the solvent, the residue was further pumped in vacuo for 1 h to give di-tert-butyl phosphorobromidate as a colorless oil (23.5 g, 86%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08088793B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-47f2d9d209f04415a33207330d3d3ad2
Quellennotizuspto-grants-2012_01