Potassium Nitrate → HCID 59745249, compound
Reaction equation
[CH2:1]([O:3][C:4](=[O:16])[NH:5][C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[C:11](=[O:15])[CH2:10][CH2:9]2)[CH3:2].[N+:17]([O-])([O-:19])=[O:18].[K+]>S(=O)(=O)(O)O>[CH2:1]([O:3][C:4](=[O:16])[NH:5][C:6]1[C:7]([N+:17]([O-:19])=[O:18])=[C:8]2[C:12](=[CH:13][CH:14]=1)[C:11](=[O:15])[CH2:10][CH2:9]2)[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
(1-Oxo-indan-5-yl)-carbamic acid ethyl ester (0.94 g, 4.3 mmol) was dissolved in 20 ml of concentrated sulphuric acid and cooled to 0° C. using an ice-bath. Potassium nitrate (477 mg, 4.7 mmol) was added in small portions. After complete addition, the mixture was stirred for 3 hours at 0° C. and then poured onto crushed ice. The yellow precipitate was filtered off, washed thoroughly with water and dried in vacuo to give a yellow solid product (0.85, 75%).
Workup
- additionAfter complete addition
- additionpoured
- customonto crushed ice
- filtrationThe yellow precipitate was filtered off
- washwashed thoroughly with water
- customdried in vacuo
- customto give a yellow solid product (0.85, 75%)
Sources & evidence
- ORD record
- ord-7d13cc696043442287f7f6dcda2341fe
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07960436B2
Reaction notes
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