Chloromethyl Methyl Ether → HCID 67227478, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:39]=[CH:40][CH:41]=1)[O:5][C:6]1[CH:16]=[C:15]([N:17]2[CH2:22][CH2:21][N:20]([CH2:23][C:24]3[CH2:29][CH2:28][C:27]([CH3:31])([CH3:30])[CH2:26][C:25]=3[C:32]3[CH:37]=[CH:36][C:35]([Cl:38])=[CH:34][CH:33]=3)[CH2:19][CH2:18]2)[CH:14]=[CH:13][C:7]=1[C:8]([O:10][CH2:11][CH3:12])=[O:9].[CH3:42][O:43][CH2:44]Cl.C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C)C=O>[Cl:38][C:35]1[CH:34]=[CH:33][C:32]([C:25]2[CH2:26][C:27]([CH3:30])([CH3:31])[CH2:28][CH2:29][C:24]=2[CH2:23][N:20]2[CH2:19][CH2:18][N:17]([C:15]3[CH:14]=[CH:13][C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[C:6]([O:5][C:4]4[CH:39]=[CH:40][CH:41]=[C:2]([O:1][CH2:42][O:43][CH3:44])[CH:3]=4)[CH:16]=3)[CH2:22][CH2:21]2)=[CH:37][CH:36]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A suspension of EXAMPLE 176B (0.295 g), methoxymethyl chloride (0.117 mL) and cesium carbonate (0.334 g) in N,N-dimethylformamide (3 mL) was stirred at 60° C. for 16 hours. The reaction mixture was partitioned between dichloromethane and water. The water layer was extracted with dichloromethane. The combined organic extracts were washed with water (2×), dried over magnesium sulfate, filtered and concentrated. The crude product was purified by flash chromotography (silica gel, 5%-20% ethyl acetate/hexanes) providing the product.
Workup
- customThe reaction mixture was partitioned between dichloromethane and water
- extractionThe water layer was extracted with dichloromethane
- washThe combined organic extracts were washed with water (2×)
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customThe crude product was purified by flash chromotography (silica gel, 5%-20% ethyl acetate/hexanes)
- customproviding the product
Sources & evidence
- ORD record
- ord-dd8b080e6de7486fa66f29c8ac202584
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08557983B2
Reaction notes
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