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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041508Generated: October 30, 2026

tert-Butyl mercaptan → 6-(tert-butylsulfanyl)pyridine-3-carbonitrile

https://huagongshe.com/reaction/2041508

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl mercaptanHCID 6387—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium ethoxideHCID 2723922—
Reactant6-Chloro-3-pyridinecarbonitrileHCID 5152094—
SolventEthanolHCID 702—
Product6-(tert-butylsulfanyl)pyridine-3-carbonitrileHCID 2841319091.2%

Reaction Steps

Add sodium ethoxide (12 mL of 21% w/v in ethanol, 36 mmol) to a solution of 2-methyl-2-propanethiol (4.06 mL, 36 mmol) in anhydrous ethanol (90 mL) at 0° C. under nitrogen atmosphere. Stir the solution and allow it to warm to room temperature over 30 min. Add 6-chloronicotinonitrile (5 g, 36 mmol) and then heat the reaction to reflux overnight. Cool to room temperature, add saturated aqueous NaHCO3 and concentrate in vacuo. Extract into EtOAc or dichloromethane and wash with brine. Dry over MgSO4 and concentrate in vacuo to give the desired intermediate as orange crystals (6.31 g, 91%). MS (ES+) m/z: 193 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580780B2
Source datasetuspto-grants-2013_11
ORD IDord-5506a3c3b2a24f24980350737590ca9e
Source noteuspto-grants-2013_11