Hydrochloric Acid → HCID 12942114, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([NH:23][C:24](=[O:28])[N:25]([CH3:27])[CH3:26])[CH:5]=[CH:6][C:7]=1[O:8][CH2:9][CH2:10][CH2:11][C:12]1([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)OCC[O:13]1.O1CCCC1.Cl>[Cl-].[Na+].O>[C:12]([CH2:11][CH2:10][CH2:9][O:8][C:7]1[CH:6]=[CH:5][C:4]([NH:23][C:24](=[O:28])[N:25]([CH3:27])[CH3:26])=[CH:3][C:2]=1[Cl:1])(=[O:13])[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 3-{3-chloro-4-[3-(2-phenyl-1,3-dioxolan-2-yl)propoxy]phenyl}-1,1-dimethylurea (2.03 g; 0.005 mol), tetrahydrofuran (10 ml) and 10% aqueous hydrochloric acid (2 ml) is stirred overnight. The reaction mixture is poured into brine (100 ml) and extracted with methylene chloride. The organic layer is washed with water, dried and evaporated to afford the product: 1.69 g of an off-white solid. Recrystallization from a toluene-hexane mixture (50 ml) yields 1.33 g of cream colored needles, m.p. 129°-130° C.
Workup
- extractionextracted with methylene chloride
- washThe organic layer is washed with water
- customdried
- customevaporated
- customto afford the product
- customRecrystallization from a toluene-hexane mixture (50 ml)
- customyields 1.33 g of cream colored needles, m.p. 129°-130° C.
Sources & evidence
- ORD record
- ord-1c830e65fe2348868fcc6875ef511b3c
- Source dataset
- uspto-grants-1981_10
- Patent number
- US04294986
Reaction notes
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