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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836751Generated: October 25, 2026

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

https://huagongshe.com/reaction/1836751

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 numberUS06777433B2
Source datasetuspto-grants-2004_08
ORD IDord-9d72a0551e864d5489519bd0482b2197
Source noteuspto-grants-2004_08