Bromine → HCID 19696170, compound
Reaction equation
[N:1]([CH:4]1[CH2:13][C:12]2[C:11]([NH:14][C:15](=[O:17])[CH3:16])=[CH:10][CH:9]=[CH:8][C:7]=2[CH2:6][CH2:5]1)=[N+:2]=[N-:3].[Br:18]Br>C(O)(=O)C>[N:1]([CH:4]1[CH2:13][C:12]2[C:11]([NH:14][C:15](=[O:17])[CH3:16])=[CH:10][CH:9]=[C:8]([Br:18])[C:7]=2[CH2:6][CH2:5]1)=[N+:2]=[N-:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of N-(7-azido-5,6,7,8-tetrahydronaphthalen-1-yl)-acetamide (1 g, 4.3 mmol) in acetic acid (40 mL) was treated dropwise with bromine (1 g, 6.5 mmol) and stirred at room temperature for 3 h. The solvent was evaporated and the solid residue was washed with ether, collected by filtration and dried to give the product (1.5 g) in 89% yield.
Workup
- customThe solvent was evaporated
- washthe solid residue was washed with ether
- filtrationcollected by filtration
- customdried
Sources & evidence
- ORD record
- ord-be793dd56f2b47a18a249d2dbe8f96e4
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05721234
Reaction notes
Loading…