HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4243Generated: October 23, 2026
Aniline → 2-(2-Methylthioethoxy)-phenylhydrazine
https://huagongshe.com/en/reaction/4243
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 2-(2-Methylthioethoxy)aniline | HCID 54213163 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(2-Methylthioethoxy)-phenylhydrazine | HCID 54289290 | — |
Reaction Steps
27.4 g of the aniline obtained under (b) are placed into 45 ml of glacial acetic acid and, with ice cooling, a mixture of 37 ml of concentrated HCl and 75 ml of H2O is added. The formed suspension is diazotised at 0°-5° C. with 10.3 g of NaNO2 in 22 ml of water. The diazonium solution is subsequently stirred at 0° C. for 10 minutes, and a solution of 80.7 g of SnCl2.2H2O in 112 ml of concentrated HCl is then quickly added with cooling. After 4 hours, water is added to the reaction mixture, and extraction is repeatedly performed with ether. The aqueous phase is afterwards rendered alkaline with a 10% aqueous sodium hydroxide solution, and extracted three times with ether. After customary further processing of the ether phases, there is obtained the compound of the formula ##STR61## having a melting point of 72.5°-74.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04725302 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-8ff8d568cf1248518f7da91bcabe7759 |
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| Source note | uspto-grants-1988_02 |
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