HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76812Generated: October 27, 2026
Hydrochloric Acid → 2-(1,3-Benzothiazol-2-yl)acetonitrile
https://huagongshe.com/reaction/76812
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(1,3-Benzothiazol-2-yl)acetonitrile | HCID 342465 | — |
Reaction Steps
To a solution of malonodinitrile (13.22 g, 0.200 mole) in dry chloroform (100 mL) was added ethanol (9.2 g, 0.200 mole). Hydrogen chloride (8.0 g, 0.220 mole) was passed into the solution at room temperature and the resulting suspension was stirred for an additional 16 hours at room temperature. The excess of hydrogen chloride was removed by passing dry nitrogen into the reaction mixture. A solution of o-aminothiophenol (25 g, 0.200 mole) in chloroform was added to the reaction mixture dropwise during 30 min and the reaction mixture was stirred for 1 hour at 60° C. After that the reaction mixture was cooled to room temperature, washed with water (2×100 mL) and dried with magnesium sulfate. Chloroform was removed using a rotary evaporator. The solid residue was recrystallized from ethyl alcohol. White crystals. The yield was 26.1 g (75% of theory). Mp=101-103° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835632B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-cdc4ba3541b0469686af654ff80cee83 |
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| Source note | uspto-grants-2014_09 |
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