3-Butyn-1-OL → HCID 19373391, compound
Reaction equation
[H-].[Na+].[CH2:3]([OH:7])[CH2:4][C:5]#[CH:6].Br[CH2:9][CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12]>C1(C)C=CC=CC=1>[CH2:3]([O:7][CH2:9][CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH2:4][C:5]#[CH:6]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Sodium hydride (4.6 g of 60% dispersion in mineral oil) was added to a stirred solution of but-3-yn-1-ol (16.2 g, 0.23 mol, Lancaster) in dry toluene (200 ml). After stirring for 2 hours at 25° C. a solution of ethyl 3-bromopropionate (20.8 g, 0.115 mol, Lancaster) was added. The reaction mixture was stirred and refluxed for 7 hours. Ethyl 3-(but-3-ynyloxy)propionate (17.8 g) was obtained by quenching the cooled reaction mixture in water, extracting with ether, washing with brine, drying over anhydrous magnesium sulphate followed by evaporation.
Workup
- additionwas added
- temperaturerefluxed for 7 hours
Sources & evidence
- ORD record
- ord-0489bf315dc5496e81981329f1b669af
- Source dataset
- uspto-grants-1992_05
- Patent number
- US05116862
Reaction notes
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