Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | HCID 19791150 | HCID 19791150 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19791196 | HCID 19791196 | — |
Reaction Steps
3,4 -dichloro-5 -methyl-2 -hydroxymethylpyridine (4 g) was dissolved in 33 % dimethylamine in ethanol (11 ml), placed in a sealed vessel and heated to 2000° C. for 4 hours. On cooling, the reaction mixture was evaporated under reduced presure and the residue dissolved in water (15 ml) and ether extracted. Etherial extracts were dried (K2CO3 ), filtered and stripped to yield 4 -dimethylamino-3 -chloro-5 -methyl-2 -hydroxymethylpyridine, 4.08 g as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05250527 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-1710ec3cb6394729bfec9f19484f7859 |
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| Source note | uspto-grants-1993_10 |
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