Potassium Hydroxide → HCID 14574099, compound
Reaction equation
[OH:1][CH2:2][CH2:3][N:4]([CH2:17][CH2:18][OH:19])[C:5](=[O:16])[C:6]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[CH:9]=[CH:8][C:7]=1Cl.[OH-].[K+]>O>[N+:12]([C:10]1[CH:9]=[CH:8][C:7]2[O:1][CH2:2][CH2:3][N:4]([CH2:17][CH2:18][OH:19])[C:5](=[O:16])[C:6]=2[CH:11]=1)([O-:14])=[O:13]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 10 °C
Procedure
144.5 g of N,N-bis(2-hydroxyethyl)-2-chloro-5-nitrobenzamide in 500 ml of water containing 28 g of potassium hydroxide are heated for 2 hours with reflux cooling. The mixture is cooled to 10° C. and the precipitated, single-substance product is filtered off with suction and dried. 84 g of 7-nitro-4-(2-hydroxyethyl)-2,3-dihydro-1,4-benzoxazepin-5-one of melting point 151° C. are obtained. ##STR22##
Workup
- temperaturewith reflux
- temperaturecooling
- filtrationthe precipitated, single-substance product is filtered off with suction
- customdried
Sources & evidence
- ORD record
- ord-11ae5788d12749a39038a3be7bae2240
- Source dataset
- uspto-grants-1992_06
- Patent number
- US05126481
Reaction notes
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