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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722734Generated: October 31, 2026

Acetic Acid → Methyl 2-isocyano-2-(2-thienylmethyl)butyrate

https://huagongshe.com/reaction/1722734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-(Bromomethyl)thiopheneHCID 11829978—
ReactantMethyl 2-isocyanobutyrateHCID 16754012—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-isocyano-2-(2-thienylmethyl)butyrateHCID 2002742788.5%

Reaction Conditions

Temperature-30 °C

Reaction Steps

A suspension of potassium tert.-butoxide (5.5 g) in tetrahydrofuran (50 ml) is cooled to -30° C., and a solution of methyl 2-isocyanobutyrate (5.5 g) in tetrahydrofuran (10 ml) is added dropwise to the suspension at -30° C. The mixture is stirred at the same temperature for 30 minutes and a solution of 2-bromomethylthiophene (6.9 g) in tetrahydrafuran (10 ml) is added dropwise to the mixture. The mixture is stirred at room temperature for 4 hours, adjusted to pH 7 with acetic acid and then concentrated under reduced pressure to remove solvent. The residue is dissolved in a mixture of ethyl acetate and water and the organic layer is collected therefrom. The organic layer is washed with an aqueous saturated sodium chloride solution, dried and concentrated to remove solvent. The residue is distilled under reduced pressure, whereby methyl 2-isocyano-2-(2-thienylmethyl)butyrate (7.7 g) is obtained as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04857543
Source datasetuspto-grants-1989_08
ORD IDord-759e756f67714c06833db969e245f1ad
Source noteuspto-grants-1989_08