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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62865Generated: October 25, 2026

Cyclohexyl bromide → 2-Cyclohexylsulfanyl-nicotinic acid

https://huagongshe.com/reaction/62865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl bromideHCID 7960—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178524460HCID 178524460—
SolventDimethylformamideHCID 6228—
Product2-Cyclohexylsulfanyl-nicotinic acidHCID 28738802—

Reaction Steps

2-Mercapto-nicotinic acid (0.5 g, 3.22 mmol) was dissolved in DMF (5 mL), and the solution was cooled to 0˜5° C. NaH (0.64 g, 16.11 mmol) was added slowly thereto, and the mixture was stirred at 0˜5° C. for 30 minutes. Bromo-cyclohexane (1.19 mL, 9.66 mmol) was added thereto, and the mixture was stirred at room temperature for 12 hours. After the termination of the reaction, the reactant was concentrated under reduced pressure, and the residue was diluted with water. 3N HCl was used to adjust the pH of the solution to 2˜3, and the solution was extracted with EtOAc. The organic layer was dried with MgSO4 and concentrated under reduced pressure to obtain the title compound, which was used in the next step without a separate purification process.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447044B2
Source datasetuspto-grants-2016_09
ORD IDord-c254a23b3b1a4858b03651e3dddb1ae7
Source noteuspto-grants-2016_09