Sodium Hydroxide → Urea

反応式

[C:1]([NH:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:8](Br)=[CH:7][C:6]=1[N+]([O-])=O)(=[O:3])C.[OH-].[Na+].BrC1C2C(=CC=CC=2)C(O)=C([N+:33]([O-])=O)C=1>>[NH2:33][C:1]([NH2:4])=[O:3].[N:4]1[C:5]2[C:14]3[C:9]([CH:8]=[CH:7][C:6]=2[O:3][CH:1]=1)=[CH:10][CH:11]=[CH:12][CH:13]=3

参加物

反応物 3

HCID 14798Sodium Hydroxide

HCID 3484101-(acetylamino)-4-bromo-2-nitronaphtalene

HCID 115725344-Bromo-2-nitronaphthalen-1-ol

生成物 2

HCID 1176Urea

HCID 3718558Naphth[1,2-d]oxazole

実験手順

When 1-(acetylamino)-4-bromo-2-nitronaphtalene was treated with aqueous sodium hydroxide as described above the product was 4-bromo-2-nitro-1-naphtol—i.e. substitution occurred instead of hydrolysis. Subsequent hydrogenation and treatment with urea yielded naphto[1,2-d]oxazoline in 44% overall yield.