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HRID 1836751作成日:2026年10月25日

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

https://huagongshe.com/reaction/1836751

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium AcetateHCID 517165—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物2-Bromo-4-(bromomethyl)benzaldehydeHCID 12016038—
反応物Di-tert-butyl phosphiteHCID 21959072—
溶媒TetrahydrofuranHCID 8028—
生成物Di(tert-butyl) [2-bromo-4-(bromomethyl)phenyl](hydroxy)methylphosphonateHCID 1201603989%

反応条件

温度-78 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06777433B2
出典データセットuspto-grants-2004_08
ORD IDord-9d72a0551e864d5489519bd0482b2197
出典メモuspto-grants-2004_08