Hydrogen Bromide → HCID 67804523, compound
Reaction equation
[OH:1][C:2]1[C:13]([N+:14]([O-:16])=[O:15])=[CH:12][C:5]([CH2:6][C@@H:7]([C:9]([OH:11])=[O:10])[NH2:8])=[CH:4][C:3]=1[O:17]C.[BrH:19]>>[BrH:19].[OH:17][C:3]1[CH:4]=[C:5]([CH:12]=[C:13]([N+:14]([O-:16])=[O:15])[C:2]=1[OH:1])[CH2:6][C@@H:7]([C:9]([OH:11])=[O:10])[NH2:8]Participants
3
Procedure
A solution containing 1.2 g of 4-hydroxy-3-methoxy-5-nitrophenylalanine hydrosulfate in 10 ml of conc. hydrobromic acid was refluxed for 2 h. The solution was concentrated in vacuo and allowed to stand over night in a refrigerator. The product was filtered and washed with hydrobromic acid and dried. Yield 0.25 g, m.p. 170° C. (decomp.).
Workup
- temperaturewas refluxed for 2 h
- concentrationThe solution was concentrated in vacuo
- waitto stand over night in a refrigerator
- filtrationThe product was filtered
- washwashed with hydrobromic acid
- customdried
Sources & evidence
- ORD record
- ord-493a296204fd4d6aafa0c51a52168bcd
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05446194
Reaction notes
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