Hydrochloric Acid → HCID 21444156, compound
Reaction equation
[OH-].[Na+].O.[N+:4]([C:7]1[CH:8]=[C:9]([CH2:17][C:18]([O:20]C)=[O:19])[CH:10]=[CH:11][C:12]=1[O:13][CH2:14][C:15]#[CH:16])([O-:6])=[O:5].Cl>CO>[N+:4]([C:7]1[CH:8]=[C:9]([CH2:17][C:18]([OH:20])=[O:19])[CH:10]=[CH:11][C:12]=1[O:13][CH2:14][C:15]#[CH:16])([O-:6])=[O:5]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
In a mixed solution of 0.5g of sodium hydroxide, 5 ml of water and 2ml of metanol 0.7g of methyl 3-nitro-4-propargyloxyphenylacetate was added and heated on a water bath for 30 minutes. After cooling, the solution was neutralized with 10% hydrochloric acid and the thus obtained crystals were recrystallized from ether-n-hexane to give the object compound having m.p. 135° - 137° C in a yield of 0.6g (90.6%).
Workup
- temperatureheated on a water bath for 30 minutes
- temperatureAfter cooling
- customthe thus obtained crystals were recrystallized from ether-n-hexane
- customto give the object compound
Sources & evidence
- ORD record
- ord-3410ea1ec9074bf5b3ef87e5ec5350da
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04016193
Reaction notes
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