Methanol → HCID 20335783, compound
Reaction equation
[C:1]([C:9]1[C:14]([N+:15]([O-:17])=[O:16])=[CH:13][CH:12]=[C:11](Cl)[N:10]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Na].[CH3:20][OH:21]>O>[C:1]([C:9]1[C:14]([N+:15]([O-:17])=[O:16])=[CH:13][CH:12]=[C:11]([O:21][CH3:20])[N:10]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
60 grams of 2-benzoyl-3-nitro-6-chloropyridine were added in portions to a solution of 10 grams of sodium metal in 500 ml. of methanol at 50° C. with stirring, whereby the temperature gradually increased. Then the mixture was heated under reflux for four hours and subsequently treated with two liters of water. The precipitated crystals were filtered off with suction after one hour and recrystallized from methanol.
Workup
- temperaturewhereby the temperature gradually increased
- temperatureThen the mixture was heated
- temperatureunder reflux for four hours
- filtrationThe precipitated crystals were filtered off with suction after one hour
- customrecrystallized from methanol
Sources & evidence
- ORD record
- ord-d40e677dbfbe4c6b9e91a0849298cbb6
- Source dataset
- uspto-grants-1980_06
- Patent number
- US04207322
Reaction notes
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