Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194942Generated: November 2, 2026

Potassium Carbonate → HCID 59637265, compound

https://huagongshe.com/reaction/2194942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenyl chloroformateHCID 15891—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant(3-tert-butyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl)methanamineHCID 58093530—
SolventDimethylformamideHCID 6228—
ProductHCID 59637265HCID 5963726546.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (3-tert-butyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl)methanamine (5 g, 0.018 mol) in DMF (25 ml, 5 times), potassium carbonate (9.16 g, 0.066 mol, 3.5 eq) was added and cooled the contents to 0° C. Then phenyl chloroformate (3.28 g (2.65 ml), 0.02 mol, 1.1 eq) was added drop wise for 15 min and the overall reaction mixture was stirred for another 15 min at 0° C. Progress of the reaction was monitored by TLC (20% ethyl acetate/hexane, Rf˜0.3). On completion of the reaction, reaction contents were filtered, filtrate was diluted with cold water (100 ml) and the product extracted with ethyl acetate (3×25 ml). Combined organic layer was washed with brine solution (100 ml), dried over sodium sulfate and concentrated under reduced pressure. Crude obtained was purified by column chromatography (silica gel, 10% ethyl acetate/hexane) to yield the required product as a white solid (3.2 g, 45% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334315B2
Source datasetuspto-grants-2012_12
ORD IDord-ecd2d30141a942efa5b14f8403deba12
Source noteuspto-grants-2012_12