Potassium Hydroxide → HCID 13491773, compound
Reaction equation
[CH3:1][C:2]1[C:7]([OH:8])=[C:6]([CH2:9][OH:10])[C:5]([CH:11](Br)[CH2:12]Br)=[CH:4][N:3]=1.[OH-].[K+]>>[CH3:1][C:2]1[C:7]([OH:8])=[C:6]([CH2:9][OH:10])[C:5]([C:11]#[CH:12])=[CH:4][N:3]=1Participants
3
Procedure
The oily product from Step A was refluxed in 15 ml. of 10% (w/v) ethanolic potassium hydroxide under nitrogen for 10 minutes. After cooling the solvent was evaporated. The residue was extracted with 2×20 ml. of hot isopropanol which was then filtered and evaporated to give solid 2-methyl-3-hydroxy-4-hydroxymethyl-5-ethynylpyridine, m.p. 170°-171° C.
Workup
- temperatureAfter cooling the solvent
- customwas evaporated
- extractionThe residue was extracted with 2×20 ml
- filtrationof hot isopropanol which was then filtered
- customevaporated
Sources & evidence
- ORD record
- ord-3fb5656036124302ad994dd0ad4d3de1
- Source dataset
- uspto-grants-1982_10
- Patent number
- US04355034
Reaction notes
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