Acetic Anhydride → 1,2,3,4-Tetrahydro-4-acetoxy-1-naphthylurea
Reaction equation
[C:1]([O:4][C:5](=[O:7])[CH3:6])(=O)[CH3:2].OC1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:12]([NH:19][C:20]([NH2:22])=[O:21])[CH2:11]C1>O>[C:5]([O:4][CH:1]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:12]([NH:19][C:20]([NH2:22])=[O:21])[CH2:11][CH2:2]1)(=[O:7])[CH3:6]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To 10 ml of acetic anhydride 2.0 g of 1,2,3,4-tetrahydro-4-hydroxy-1-naphthylurea (cis/trans) is added and the mixture stirred for 1 hour. The mixture is poured into water and the title compound collected by filtration. Evaporation of the mother liquor in vacuo affords additional title compound.
Workup
- filtrationthe title compound collected by filtration
- customEvaporation of the mother liquor in vacuo
Sources & evidence
- ORD record
- ord-270246bffdbe4dbcb0c77ca9061c1b8d
- Source dataset
- uspto-grants-1978_05
- Patent number
- US04089976
Reaction notes
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