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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373791Generated: October 30, 2026

Ethyl Acetate → BM 11

https://huagongshe.com/reaction/373791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCyclohexyl isothiocyanateHCID 14289—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 15135616HCID 15135616—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
SolventPropan-2-one--water (1/1)HCID 18366337—
ProductBM 11HCID 303608350%

Reaction Steps

0.01 mol of NaOH dissolved in a minimum of water is added to a solution of 0.01 mol of (4-(cycloheptylamino)pyrid-3-yl)sulfonamide in 80 ml of a water/acetone mixture (1:1). The mixture is stirred with a magnetic rod, and 0.015 mol of cyclohexylisothiocyanate is added. Stirring is continued, while the reaction is followed by TLC (silica gel 60F254; mobile phase: ethyl acetate 9, methanol 1, triethylamine 0.2). Gentle heating can accelerate the reaction. The mixture is evaporated under reduced pressure and the residue is taken up in 100 ml of 0.2N NaOH. Any insoluble material is filtered out and the solution is corrected to pH 6.5-7 and left to crystallize for 1 hour in the refrigerator. The precipitate collected is suspended in 100 ml of a water/acetone mixture (4:1) saturated with NaHCO3. The mixture is stirred for 1 hour and then filtered, and the filtrate, brought back to pH 6.5-7, is left to crystallize in the refrigerator. The crystals are collected, washed in cold water and dried under vacuum at normal temperature. Yield is around 50-60%. Melting point: 195°-197° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166162
Source datasetuspto-grants-1992_11
ORD IDord-c109f0f0a3b64d8fbc4956c62e237afc
Source noteuspto-grants-1992_11