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HRID 746065作成日:2026年10月27日

Diethyl Ether → [Ethoxy(4-phenylbutyl)phosphoryl]acetic acid

https://huagongshe.com/reaction/746065

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Bromoacetic AcidHCID 6227—
反応物ChlorotrimethylsilaneHCID 6397—
反応物TriethylamineHCID 8471—
反応物4-Phenylbutylphosphonous acidHCID 13274665—
溶媒ChloroformHCID 6212—
生成物[Ethoxy(4-phenylbutyl)phosphoryl]acetic acidHCID 1313684897%

反応条件

温度0 °C

反応手順

To a solution of 4-phenylbutyl phosphonous acid, ethyl ether (0.5 g, 0.0022 mole) in chloroform (10 ml) was added triethylamine (0.68 ml, 0.0048 mole) and the solution was cooled in an ice bath to 0° C. Trimethyl silyl chloride (0.6 ml, 0.0048 mole) was added to the above solution dropwise, followed by bromoacetic acid (0.34 g, 0.0024 mole). The ice bath was removed and the mixture stirred at room temperature for 5 hours and poured into 10% aqueous HCl (30 ml) and crushed ice (20 g). After shaking the mixture in a separatory funnel, the chloroform layer was separated and the aqueous layer extracted with dichloromethane (2×50 ml). The combined organic phase was washed with brine, dried over anhydrous sodium sulfate and the solvents removed on a rotavap. The resulting crude thick oil was vacuum dried to get 0.61 g (97%) of title compound in the form of an oil, TLC: Silica gel, CH2Cl2 :MeOH:HOAc shows one main spot at Rf =0.37.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04602092
出典データセットuspto-grants-1986_07
ORD IDord-1f460e3036be4135ae4478e6628ba798
出典メモuspto-grants-1986_07