HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619073Generated: October 31, 2026
Thiourea → 3-(2-Amino-thiazol-4-yl)-benzonitrile
https://huagongshe.com/reaction/619073
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 3-(2-Bromoacetyl)benzonitrile | HCID 2735867 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(2-Amino-thiazol-4-yl)-benzonitrile | HCID 2756558 | — |
Reaction Steps
16.9 g of 3-bromoacetyl-benzonitrile were placed in 50 ml of methanol and treated at room temperature with 8 g of thiourea. The mixture was boiled for 21/2 hours and then cooled to 0° C. while stirring slowly. The product separated as the salt, was filtered off and converted into the base by the addition of 100 ml of 2N sodium hydroxide solution. The aqueous suspension was extracted with a total of 700 ml of methylene chloride and the organic phase was dried with magnesium sulphate. 9.6 g of 3-(2-amino-thiazol-4-yl)-benzonitrile separated upon concentration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05958910 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-c619c38e7f764e81ae870da8f49dac2f |
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| Source note | uspto-grants-1999_09 |
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