HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990067Generated: November 2, 2026
Triethylamine → Ethyl 3-amino-4-cyano-5-(methylsulfanyl)thiophene-2-carboxylate
https://huagongshe.com/reaction/1990067
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Reactant | 2-(Bis(methylsulfanyl)methylidene)propanedinitrile | HCID 99229 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-amino-4-cyano-5-(methylsulfanyl)thiophene-2-carboxylate | HCID 474798 | — |
Reaction Steps
Stir a slurry of bis(methylthio)methylenepropanedinitrile, prepared in preparation 34, (69.29 g, 407 mmol) in ethanol (1.1 L) under nitrogen at rt then add ethyl thioglycolate (44.9 mL, 407 mmol) followed by triethylamine (56.7 mL, 407 mmol). Heat the resulting mixture at 65° C. for 30 min. Cool slowly to 35° C. over 45 min, then cool to 3° C. over 20 min and maintain at that temperature for 20 min. Collect precipitate by filtration, wash with cold ethanol and ether to afford the title compound: 1H NMR (CDCl3) δ 5.77 (bs, 2H), 4.28 (q, J=7.1, 2H), 2.64 (s, 3H), 1.33 (t, J=7.1, 3H); TLC (25% hexanes/ethyl acetate) Rf=0.25).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642361B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-c1ad053fdf984875abe58c9b1923611a |
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| Source note | uspto-grants-2010_01 |
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