Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051981Generated: October 26, 2026

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

https://huagongshe.com/reaction/1051981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl AcetateHCID 7915—
ReactantSodium BicarbonateHCID 516892—
ReactantChloromethyl chlorosulfateHCID 2733556—
ReactantPotassium di-tert-butyl phosphateHCID 23674467—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
ProductDi-tert-butyl (chloromethyl) phosphateHCID 1170163090%

Reaction Conditions

Temperature35 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388203B2
Source datasetuspto-grants-2016_07
ORD IDord-c96ff090b8de4b54afaedfbba6baad46
Source noteuspto-grants-2016_07