Potassium → HCID 68118258, compound
Reaction equation
Cl.[NH2:2][CH2:3][CH:4]([OH:17])[CH2:5][O:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[O:13][CH2:14][CH:15]=[CH2:16].[K].[C:19]([CH:27]=[C:28](O)[CH3:29])(=[O:26])[C:20]1[CH:25]=[CH:24][CH:23]=[N:22][CH:21]=1>C(O)C>[C:19]([CH:27]=[C:28]([NH:2][CH2:3][CH:4]([OH:17])[CH2:5][O:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[O:13][CH2:14][CH:15]=[CH2:16])[CH3:29])(=[O:26])[C:20]1[CH:25]=[CH:24][CH:23]=[N:22][CH:21]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
5.1 g of 1-amino-3-(o-allyloxyphenoxy)-propan-2-ol hydrochloride ##STR30## are suspended in 50 ml of ethanol, 4 g of the potassium salt of 2-nicotinoyl-1-methyl-vinyl alcohol ##STR31## are then added and the mixture is stirred for 24 hours at room temperature. The suspension is filtered off and the residue is washed with ethanol. The filtrate, together with the wash alcohol is concentrated in vacuo. An oil is left, which solidifies after a short time. The oil which has solidified, together with the residue left on washing with alcohol, is repeatedly triturated with water and then recrystallised from ethanol. 1-(2-Nicotinoyl-1-methyl-vinylamino)-3-(o-allyloxyphenoxy)-propan-2-ol of the formula ##STR32## is thus obtained.
Workup
- filtrationThe suspension is filtered off
- washthe residue is washed with ethanol
- concentrationThe filtrate, together with the wash alcohol is concentrated in vacuo
- waitAn oil is left
- waitleft
- washon washing with alcohol
- customis repeatedly triturated with water
- customrecrystallised from ethanol
Sources & evidence
- ORD record
- ord-f5adee1185234ead9e9b26434cb64cbb
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04018778
Reaction notes
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