Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186711Generated: November 3, 2026

Cesium carbonate → Methyl 5-((tert-butyldimethylsilyloxy)methyl)-3-phenylthiophene-2-carboxylate

https://huagongshe.com/reaction/1186711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantMethyl ThioglycolateHCID 16907—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant4-{[Tert-butyl(dimethyl)silyl]oxy}-1-phenylbut-2-yn-1-oneHCID 10869508—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 5-((tert-butyldimethylsilyloxy)methyl)-3-phenylthiophene-2-carboxylateHCID 66863649—

Reaction Steps

To a solution of 167 (8.924 g, 32.5 mmol) in THF was added methyl thioglycolate (4.36 mL, 48.8 mmol) and stirred 2 hours at room temperature. MAGNESIUM SULFATE (3.91 g, 32.5 mmol) was added and the reaction mixture was stirred for 1 hour. Then CESIUM CARBONATE (10.60 g, 32.5 mmol) in 30 mL of MeOH was added and stirred for an additional 2 hours at room temperature. The reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with brine, dried over sodium sulfate and filtered. The solvent was evaporated and the residue was purified by silica gel chromatography (0%-5% ethyl acetate in hexanes) to yield 168 in 54% (6.389 g) as an orange solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673911B2
Source datasetuspto-grants-2014_03
ORD IDord-831f253868a741158a66a8f91f556976
Source noteuspto-grants-2014_03