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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-(Bromomethyl)thiophene | HCID 11829978 | — |
| Reactant | Methyl 2-isocyanobutyrate | HCID 16754012 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-isocyano-2-(2-thienylmethyl)butyrate | HCID 20027427 | 88.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04857543 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-759e756f67714c06833db969e245f1ad |
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| Source note | uspto-grants-1989_08 |
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