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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881859Generated: November 2, 2026

Sodium methanethiolate → HCID 59331532, compound

https://huagongshe.com/reaction/1881859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
ReactantEthyl 2-(6-chloropyridin-3-yl)acetateHCID 15661146—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59331532HCID 5933153240.2%

Reaction Steps

To a solution of ethyl (6-chloropyridin-3-yl)acetate (10.7 g) in N,N-dimethylformamide (100 mL) was added sodium methanethiolate (11.3 g), and the mixture was stirred at room temperature for 23 hr. The reaction mixture was diluted with ethyl acetate, washed successively with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=5:95-50:50, volume ratio) to give the title compound (4.55 g, yield 40%) as a colorless oil. MS: 212 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318746B2
Source datasetuspto-grants-2012_11
ORD IDord-6d95e7ac57694ea1bde22f6c0e6b092e
Source noteuspto-grants-2012_11