Sodium hydride → HCID 59837297, compound
Reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([S:15][C:16]2[CH:21]=[CH:20][C:19]([CH:22](C)[CH2:23][CH:24](O)[CH:25]([NH:28][C:29]([O:31][C:32](C)(C)C)=[O:30])[CH2:26][OH:27])=[C:18]([Cl:38])[CH:17]=2)[CH:12]=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+]>C1COCC1>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([S:15][C:16]2[CH:21]=[CH:20][C:19]([CH2:22][CH2:23][CH2:24][C:25]3([CH2:26][OH:27])[CH2:32][O:31][C:29](=[O:30])[NH:28]3)=[C:18]([Cl:38])[CH:17]=2)[CH:12]=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]propyl-2-t-butoxycarbonylamino-1,3-propanediol (3.30 g) was dissolved in THF (80 mL). At 0° C., 60% sodium hydride (600 mg) was added and the mixture was stirred at room temperature for 24 hours. To the resulting reaction mixture, ice water was added and the mixture was extracted with ethyl acetate. The extract was washed sequentially with water and a saturated aqueous solution of sodium hydroxide, and the organic phase was dried over anhydrous sodium sulfate. The solvent was removed and the residue was purified on a silica gel column chromatography (hexane:ethyl acetate=1:1 and then ethyl acetate alone) to give the desired product as a pale yellow oil (2.37 g).
Workup
- additionwas added
- extractionthe mixture was extracted with ethyl acetate
- washThe extract was washed sequentially with water
- dry with materiala saturated aqueous solution of sodium hydroxide, and the organic phase was dried over anhydrous sodium sulfate
- customThe solvent was removed
- customthe residue was purified on a silica gel column chromatography (hexane
Sources & evidence
- ORD record
- ord-01ebcfa23c4440f2bccb4f61baf7e01d
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07482491B2
Reaction notes
Loading…