HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883636Generated: October 27, 2026
Water → 2-Methyl-4-(2-methyl-5-phenylbenzyl)semicarbazide
https://huagongshe.com/reaction/1883636
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Product | 2-Methyl-4-(2-methyl-5-phenylbenzyl)semicarbazide | HCID 17834941 | — |
Reaction Steps
1.0 g (4.61 mmol) of 2-methyl-5-phenylbenzyl chloride (produced in the same manner as in Intermediate Production Example 10) is dissolved in 2 ml of anhydrous N,N-dimethylformamide, and to this solution is added 450 mg (6.92 mmol) of sodium cyanide, and the mixture is stirred at 100° C. Subsequently, 2 ml of toluene is added to the reaction solution and the mixture is cooled to 0° C., to this is added 213 mg (4.61 mmol) of methylhydrazine, the mixture is stirred at room temperature, then, to this is added water, and the mixture is extracted with chloroform. The organic layer is washed with saturated saline, end-dried over anhydrous magnesium sulfate, and concentrated to obtain 2-methyl-4-(2-methyl-5-phenylbenzyl) semicarbazide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06762197B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-891aca8b8f024b228b0c61f0fb8ada3f |
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| Source note | uspto-grants-2004_07 |
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