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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952574Generated: November 2, 2026

Methanol → 5-Diethoxymethyl-3-trifluoromethyl-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1952574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethyl ThioglycolateHCID 16907—
Reactant5,5-Diethoxy-1,1,1-trifluoro-pent-3-yn-2-oneHCID 10977093—
ReactantCs2CO3 MgSO4HCID 86671257—
SolventTetrahydrofuranHCID 8028—
Product5-Diethoxymethyl-3-trifluoromethyl-thiophene-2-carboxylic acid methyl esterHCID 6822651363.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5,5-Diethoxy-1,1,1-trifluoro-pent-3-yn-2-one (2.16 g, 9.64 mmol) in THF (30 ml) was cooled to 0° C. (ice bath). Methyl thioglycolate (0.88 ml, 9.64 mmol) was added in one portion and the mixture was stirred at 0° C. for 1.5 h. Methanol (6 ml) and Cs2CO3/MgSO4 (2 g/4 g, pre-dried at 200° C. in vacuum) were added at 0° C. The mixture was stirred at 0° C. for 15 min and then at rt for 15 h. The reaction mixture was quenched by pouting into EtOAc. The organic layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by flash chromatography with 0-30% EtOAc in hexane to afford the desired product (1.90 g, 63% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404859B2
Source datasetuspto-grants-2013_03
ORD IDord-d691021b643e4f34b5014cb9c3d6edda
Source noteuspto-grants-2013_03