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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039734Generated: October 30, 2026

Ethanethiol → 6-Chloro-2-ethylsulfanyl-4-methyl-pyridine-3-carboxylic acid

https://huagongshe.com/reaction/1039734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantSodium hydrideHCID 24758—
Reactant2,6-Dichloro-4-methylpyridine-3-carboxylic acidHCID 676121—
SolventTetrahydrofuranHCID 8028—
Product6-Chloro-2-ethylsulfanyl-4-methyl-pyridine-3-carboxylic acidHCID 8666431295%

Reaction Conditions

Temperature0 °C

Reaction Steps

6.1 g (153 mmol, 60% w/w in mineral oil) NaH were dissolved in THF (90 ml) at 0° C. At this temperature 3.4 g (54.7 mmol) ethane thiol were added. After stirring for 15 min at 0° C., 12.4 g (60.2 mmol) 2,6-dichloro-4-methyl-pyridine-3-carboxylic acid were added portionwise. The RM was allowed to warm to RT and stirring was continued at RT for 16 h. Then the reaction was quenched with a 2M aq. HCl and diluted with EtOAc. The organic layer was separated, dried over MgSO4 and concentrated in vacuo. Crystallisation (DCM/hexane) of the residue yielded 12.0 g (51.7 mmol, 95%) 6-chloro-2-ethylsulfanyl-4-methyl-pyridine-3-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552200B2
Source datasetuspto-grants-2013_10
ORD IDord-2db5ef4255ef4ddf8171a4e0ec27f0ff
Source noteuspto-grants-2013_10