1-Chloropropane → HCID 56623178, compound
Reaction equation
C1(C([O:14][C:15]([C:17]23[C:28]4([CH:30]=[O:31])[CH2:29][CH:20]([C:21]2([CH2:33][O:34][C:35]25[CH:44]([O:45][Si:46]([C:49]([CH3:52])([CH3:51])[CH3:50])([CH3:48])[CH3:47])[CH:41]6[CH:42]([OH:43])[CH:37]([CH:38]([O:40]6)[O:39]2)[O:36]5)[CH2:22][CH:23]2[CH:27]4[CH2:26][CH2:25][CH:24]2[CH3:32])[CH:19]=[C:18]3[CH:53]([CH3:55])[CH3:54])=[O:16])C2C=CC=CC=2)C=CC=CC=1.[H-].[Na+].Cl[CH2:59][CH2:60][CH3:61]>CN(C)C=O>[CH3:59][C:60]([O:14][C:15]([C:17]12[C:28]3([CH:30]=[O:31])[CH2:29][CH:20]([C:21]1([CH2:33][O:34][C:35]14[CH:44]([O:45][Si:46]([C:49]([CH3:50])([CH3:52])[CH3:51])([CH3:47])[CH3:48])[CH:41]5[CH:42]([O:43][CH2:22][CH2:21][CH3:33])[CH:37]([CH:38]([O:40]5)[O:39]1)[O:36]4)[CH2:22][CH:23]1[CH:27]3[CH2:26][CH2:25][CH:24]1[CH3:32])[CH:19]=[C:18]2[CH:53]([CH3:55])[CH3:54])=[O:16])([CH3:61])[C:17]1[CH:28]=[CH:29][CH:20]=[CH:19][CH:18]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
50 mg of compound (6) was dissolved in 1.0 ml of dry dimethylformamide under a nitrogen atmosphere and mixed with about 4 mg of sodium hydride under cooling with ice. After 30 minutes, 56.3 μl of 1-chloropropane was added, and the reaction solution was stirred at room temperature for 3 hours. Then, the reaction solution was charged onto a silica gel column (Kieselgel 60, Merck, 1.0φ×30 cm) and eluted with n-hexane-ethyl acetate (4:1). The fraction containing the desired product was concentrated to dryness to give 21.6 mg of compound (30).
Workup
- temperatureunder cooling with ice
- additionThen, the reaction solution was charged onto a silica gel column (Kieselgel 60, Merck, 1.0φ×30 cm)
- washeluted with n-hexane-ethyl acetate (4:1)
- additionThe fraction containing the desired product
- concentrationwas concentrated to dryness
Sources & evidence
- ORD record
- ord-d55e9e663e6f4545a6076eab9b40daf1
- Source dataset
- uspto-grants-2000_07
- Patent number
- US06087390
Reaction notes
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