1-Chloropropane → HCID 56623178, compound

HRID 2288077Notes

Reaction equation

HRID 2288077 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]=1

Participants

5

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

  1. temperatureunder cooling with ice
  2. additionThen, the reaction solution was charged onto a silica gel column (Kieselgel 60, Merck, 1.0φ×30 cm)
  3. washeluted with n-hexane-ethyl acetate (4:1)
  4. additionThe fraction containing the desired product
  5. 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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