HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Thioglycolate → 3-Amino-4-cyano-5-trifluoromethyl-thiophene-2-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Reactant | Fluorine | HCID 24524 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | (1-Chloro-2,2,2-trifluoroethylidene)propanedinitrile | HCID 12591685 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Amino-4-cyano-5-trifluoromethyl-thiophene-2-carboxylic acid ethyl ester | HCID 68523658 | — |
Reaction Steps
Combine 1,1-dicyano-2-chloro-2-(trifluoromethyl)ethylene (0.554 mmol) (prepared by the method of Middleton, J. Fluorine Chem., 20, 1982, p 397-418) and ethanol in a 50 ml flask. Add ethyl 2-mercaptoacetate (0.554 mmol) and potassium acetate (0.831 mmol) and heat to 60-70° C. for 30-40 minutes. Cool the reaction and add water. Product crystallizes as yellowish needles. Filter crystals and wash with 1:1 ethanol/water. Dry solid under reduced pressure to give the title compound as light yellow crystals: 1H NMR (400 MHz, CDCl3) δ 5.88 (s, 2H), 4.36 (q, 2H, J=7.2 Hz), 1.38 (t, 3H, J=7.0 Hz), MS found (M−1) 262.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07642361B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-7452cf2f27f34e108f567c0913f35af0 |
| Source note | uspto-grants-2010_01 |