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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280190Generated: October 26, 2026

Ammonium Acetate → Di(tert-butyl) [2-bromo-4-(bromomethyl)phenyl](hydroxy)methylphosphonate

https://huagongshe.com/reaction/1280190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-Bromo-4-(bromomethyl)benzaldehydeHCID 12016038—
ReactantDi-tert-butyl phosphiteHCID 21959072—
SolventTetrahydrofuranHCID 8028—
ProductDi(tert-butyl) [2-bromo-4-(bromomethyl)phenyl](hydroxy)methylphosphonateHCID 1201603989%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Di-tert-butyl phosphite (14.8 g, 76.3 mmol, 1.05 eq) was dissolved in 200 ml THF at −78° C. under nitrogen and 72 ml (1.05 eq) of 1.06M Lithium bis(trimethylsilyl)amide in THF was added over 30 min. The mixture was left stirring at −78° C. under nitrogen for 30 min and then added to a solution of the compound of Step 3 (20.2 g, 72.7 mmol, 1 eq) in 200 ml THF at −78° C. The solution was warmed to 0° C. and then poured into 400 ml of half saturated aqueous ammonium acetate. The layers were separated and the aqueous layer was washed with 400 ml isopropyl acetate. The organic layers were combined, dried with sodium sulfate and the solvent removed. The crude solid was then triturated with 15% EtOAc/hexane for 2 hours and 30.4 g (89%) of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448429B1
Source datasetuspto-grants-2002_09
ORD IDord-a07e8d6a671348bb901c4f6d64a6fc2f
Source noteuspto-grants-2002_09