HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447608Generated: October 30, 2026
N,N-Dimethylaniline → HCID 13015362, compound
https://huagongshe.com/reaction/1447608
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | 3-(Phenylsulfanyl)pyridine | HCID 3813610 | — |
| Product | HCID 13015362 | HCID 13015362 | — |
Reaction Steps
A mixture of 59.1 g. (0.316 mole) of 3-phenylthiopyridine, 14.7 g. (0.318 mole) of sodium amide and 84 gms. of dimethyl aniline is heated at 150°-160° C. for 6 hours. After dilution with 100 ml. of water, the reaction mixture is extracted with chloroform. The combined extracts are washed with water and dried. Evaporation of the solvent in vacuo yields an oily residue. The residue is triturated with three 100 ml. portions of petroleum ether yielding 17 gm. of crude insoluble product. Proton magnetic resonance spectroscopy indicates the material is a 50/50 mixture of 2- and 6-amino derivatives. The isomers are separated on silica gel eluted with 10% ethylacetate 90% methylene chloride affording pure 2-amino 3-(phenylthio) pyridine, m.p. 108°-109° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04177274 |
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| Source dataset | uspto-grants-1979_12 |
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| ORD ID | ord-705cbedf57c0445099b7b3ff5ff0f791 |
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| Source note | uspto-grants-1979_12 |
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