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HRID 1051981作成日:2026年10月23日

Isopropyl Acetate → Di-tert-butyl (chloromethyl) phosphate

https://huagongshe.com/ja/reaction/1051981

反応式

関与物質

役割名称HCID仕込み量
反応物Isopropyl AcetateHCID 7915—
反応物Sodium BicarbonateHCID 516892—
反応物Chloromethyl chlorosulfateHCID 2733556—
反応物Potassium di-tert-butyl phosphateHCID 23674467—
触媒Tetrabutylammonium hydrogen sulfateHCID 94433—
溶媒WaterHCID 962—
生成物Di-tert-butyl (chloromethyl) phosphateHCID 1170163090%

反応条件

温度35 °C

反応手順

To a mixture of potassium ditert-butyl phosphate (261 kg, 1.00 mol eq), tetra-n-butylammonium hydrogensulphate (18.5 kg, 0.05 mol eq) and sodium hydrogencarbonate (400 kg, 4.50 mol eq) in water (1150 kg) is added isopropyl acetate (1275 kg). The mixture is warmed to about 35° C. and then to this is added chloromethylchlorosulphate (313 kg, 1.80 mol eq) over about 4 hours. The mixture is further stirred for about 45 minutes, cooled to about 25° C. and then the layers separated. The organic phase is cooled to about 10° C. and washed twice with 2% w/v aqueous potassium hydrogencarbonate solution (2×800 kg) and then with a mixed 2% w/v potassium hydrogencarbonate and 20% w/v potassium hydrogencarbonate aqueous solution (640 kg). The resulting organic solution is then distilled at <100 mbar to half volume, maintaining the temperature below 45° C. The resulting mixture is filtered, washing the filter with isopropyl acetate (115 kg), to give the title compound as a solution, with typical solution strength of about 25% w/v and yield of about 90%. This solution is then used directly in Example 1, Step C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09388203B2
出典データセットuspto-grants-2016_07
ORD IDord-c96ff090b8de4b54afaedfbba6baad46
出典メモuspto-grants-2016_07