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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484759Generated: October 27, 2026

Sodium methanethiolate → Ethyl 1-(methylthiomethyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/1484759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactant1-Methanesulfonyloxymethyl-cyclopropanecarboxylic acid ethyl esterHCID 57466610—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl 1-(methylthiomethyl)cyclopropanecarboxylateHCID 66609952100.2%

Reaction Conditions

Temperature23 °C

Reaction Steps

Sodium methanethiolate (4.36 g, 62.30 mmol) was added to a stirred solution of ethyl 1-((methylsulfonyloxy)methyl)cyclopropanecarboxylate (6.92 g, 31.10 mmol) in N,N-dimethylformamide (62.30 mL) at 23° C. The resulting brown suspension was stirred at 23° C. for 18 h. The reaction mixture was diluted with water and extracted with diethyl ether. The combined organic layers were dried (MgSO4), filtered, and concentrated by rotary evaporation to afford the title compound as a brown oil (5.43 g, 100%): 1H NMR (300 MHz, CDCl3) δ 4.14 (q, J=7 Hz, 2H), 2.83 (s, 2H), 2.16 (s, 3H), 1.31 (dd, J=7, 4 Hz, 2H), 1.25 (t, J=7 Hz, 3H), 0.89 (dd, J=7, 4 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422278B2
Source datasetuspto-grants-2016_08
ORD IDord-f5046d2a9f164a0cacb6e0fc023e4662
Source noteuspto-grants-2016_08