HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380811Generated: November 1, 2026
Chloroacetonitrile → 3-Amino-5-phenylthiophene-2-carbonitrile
https://huagongshe.com/reaction/2380811
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | 3-Chloro-3-phenyl-2-propenenitrile | HCID 2777511 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Amino-5-phenylthiophene-2-carbonitrile | HCID 15570318 | 8% |
Reaction Steps
To a suspension of sodium sulfide (0.95 g, 12.23 mmol) in DMF (12.5 mL) was added a solution of 3-chloro-3-phenylprop-2-enenitrile (2 g, 12.23 mmol) in DMF (5 mL) at rt for 5 min and stirred the mixture at 60-70° C. for 2 h. Then chloroacetonitrile (0.77 mL, 12.23 mmol) was added dropwise to the reaction mixture and again stirred at 60-70° C. for 2 h. Then, a solution of sodium methoxide (0.66 g, 12.23 mmol) in methanol (5 mL) was added dropwise and stirring was continued for 1 h at the same temperature. The mixture was allowed to rt and poured into cold water and stirred for 15 min. The solid separated was filtered, washed with water and dried. The solid was recrystallized from hexane-chloroform to give the product as a pale brown color solid (150 mg, 8%), nip 158-160° C. 1H NMR (400 MHz, CDCl3): δ 7.52-7.54 (2H, m), 7.37-7.41 (3H, m), 6.75 (1H, s), 4.48 (2H, s); LC-MS (negative ion mode): m/z 199 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258119B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-e303b211dd224814817efa9246fc399b |
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| Source note | uspto-grants-2012_09 |
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