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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339822Generated: October 29, 2026

Cyclohexyl isothiocyanate → HCID 178431653, compound

https://huagongshe.com/reaction/339822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl isothiocyanateHCID 14289—
ReactantN-bromobutanimideHCID 67184—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 68291332HCID 68291332—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178431653HCID 17843165320.9%

Reaction Steps

A solution of 150 mg of 2-hydroxy-2-methyl-1-phenylpropane-1-sulfonamide and 97 mg of cyclohexyl isothiocyanate in 1.5 ml of NMP was admixed with 0.20 ml of a 2 N solution of sodium bis(trimethylsilyl)amide in THF. After stirring for 20 minutes, 71 mg of N-bromosuccinimide were added and the mixture was stirred at room temperature for a further 15 minutes. The reaction solution was admixed with 50 ml of water and extracted twice with 50 ml of ethyl acetate. The combined organic phases were dried over Na2SO4 and concentrated by rotary evaporation. The residue was purified in a purification laboratory by means of preparative HPLC, and the product-containing fractions were freed of the organic solvent under reduced pressure. The aqueous residue was extracted three times with dichloromethane, and the combined organic phases were dried using a phase separator cartridge (Chromabond® PTS) and concentrated by rotary evaporation. The residue was dissolved in a mixture of acetonitrile and water and lyophilized. This gave the product (46 mg) with a molecular weight of 336.4 g/mol (C17H24N2O3S); MS (ESI): m/e=337 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895547B2
Source datasetuspto-grants-2014_11
ORD IDord-7fdb04cb2c874ac394c2a36184f4743d
Source noteuspto-grants-2014_11