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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991246Generated: October 26, 2026

Potassium Carbonate → Isobutyl 4-(1,1-dioxido-4-thiomorpholinyl)-3,5-difluorophenylcarbamate

https://huagongshe.com/reaction/1991246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantIsobutyl chloroformateHCID 62365—
Reactant4-(1,1-Dioxido-4-thiomorpholinyl)-3,5-difluoroaniline tetrahydrofuranHCID 69853673—
ProductIsobutyl 4-(1,1-dioxido-4-thiomorpholinyl)-3,5-difluorophenylcarbamateHCID 9925157—

Reaction Conditions

Temperature45 °C

Reaction Steps

To a 400 L glass-lined reactor containing the 4-(1,1-dioxido-4-thiomorpholinyl)-3,5-difluoroaniline/tetrahydrofuran solutions (Step 3, 12.6 kg, 48 moles, 1.0 eq) is added a 47% potassium carbonate solution (14.1 kg, 48 moles, 1.0 eq). The mixture is heated to approximately 45° C., and isobutyl chloroformate (7.2 kg, 53 moles, 1.1 eq) is added while maintaining a reaction temperature between 45° C. and 55° C. The reaction is stirred at 45°-55° C. Once complete, the reaction is quenched by slowly adding water (45 L) over 15 minutes. The reaction mixture is cooled to 25° C. and the phases are separated. The tetrahydrofuran solution is swapped to an isopropanol (150 L)/water (50 L) suspension, and the slurry is slowly cooled to 5° C. The yellow slurry is then filtered and the cake washed with cold isopropanol (2×30 L). The yellow solids are dried with 60° C. nitrogen to give the title compound, 1H NMR (CDCl3) δ 7.02 (m, 2H), 6.81 (s, 1H), 3.95 (d, 2H), 3.60 (m, 4H), 3.17 (m, 4H), 1.97 (m, 1H), 0.94 (d, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645781B2
Source datasetuspto-grants-2010_01
ORD IDord-6cdbe3e2e6ab464294c023d3ad70cd25
Source noteuspto-grants-2010_01