Chloromethyl Methyl Ether → HCID 67227478, compound

HRID 1848850Notes

Reaction equation

HRID 1848850 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]=1

Participants

5

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

  1. customThe reaction mixture was partitioned between dichloromethane and water
  2. extractionThe water layer was extracted with dichloromethane
  3. washThe combined organic extracts were washed with water (2×)
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude product was purified by flash chromotography (silica gel, 5%-20% ethyl acetate/hexanes)
  8. customproviding the product

Sources & evidence

ORD record
ord-3c0421b581444f59ad8890cf5236b5ce
Source dataset
uspto-grants-2015_02
Patent number
US08952157B2

Reaction notes

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