HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27714Generated: October 25, 2026
3,5-Dimethylaniline → 2-[(5,7-Dimethylbenzothiazol-2-ylimino)methylene]propanedinitrile
https://huagongshe.com/reaction/27714
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,5-Dimethylaniline | HCID 7949 | — |
| Reactant | Ammonium thiocyanate | HCID 15666 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-(Ethoxymethylene)propanedinitrile | HCID 67152 | — |
| Reactant | (3,5-Dimethylphenyl)thiourea | HCID 736215 | — |
| Reactant | 5,7-Dimethyl-1,3-benzothiazol-2-amine | HCID 2049896 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-[(5,7-Dimethylbenzothiazol-2-ylimino)methylene]propanedinitrile | HCID 20433060 | 72.7% |
Reaction Steps
- 2-Amino-5,7-dimethylbenzothiazole was prepared by treatment of 3,5-dimethylaniline with ammonium thiocyanate and conversion of the resulting N-(3,5-dimethylphenyl) thiourea with bromine and chloroform (Barnikow and Bodeker Ber. 100(5), 1394), m.p. 142°-144°. 2-Amino-5,7-dimethylbenzothiazole, 6.16 g. (34.5 millimoles) was added to a solution of a pea-sized piece of sodium in 40 ml. of anhydrous ethanol. Ethoxymethylenemalononitrile, 4.22 g. (34.5 millimoles), was added to the solution and the mixture was heated at reflux for about 2 hrs. The precipitated solid was collected by filtration, washed with ethanol, and dried in vacuo at 100°, yielding 6.93 g. (72.7%) of the desired product which was a yellow solid, m.p. 239°-241°. A small portion was recrystallized from 95% ethanol and submitted for analysis, m.p. 241°-243°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04223031 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-8b7ecfda7b2d405987ded474fa5b4eb7 |
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| Source note | uspto-grants-1980_09 |
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