Sodium hydride → HCID 117993606, compound

HRID 571127Notes

Reaction equation

HRID 571127 reaction equation
[CH3:1][O:2][C:3](=[O:14])[CH:4](P(OCC)(OCC)=O)[CH3:5].[H-].[Na+].[C:17]([O:21][C:22]([C:24]1[S:25][C:26]([CH:29]=O)=[CH:27][CH:28]=1)=[O:23])([CH3:20])([CH3:19])[CH3:18]>O1CCCC1>[C:17]([O:21][C:22]([C:24]1[S:25][C:26](/[CH:29]=[C:4](/[C:3]([O:2][CH3:1])=[O:14])\[CH3:5])=[CH:27][CH:28]=1)=[O:23])([CH3:20])([CH3:19])[CH3:18]

Participants

5

Procedure

2-(Diethylphosphono)propanoic acid methyl ester (23.0 g, 0.103 mol) was dissolved in tetrahydrofuran (150 mL), 60% sodium hydride (2.4 g, 0.06 mol) was added at 0° C., and the mixture was stirred for 30 minutes. To the reaction mixture was added a solution of 5-formyl-2-thiophenecarboxylic acid tert-butyl ester obtained in Example 1, step 2(11.0 g, 0.052 mol) in tetrahydrofuran (10 mL), and the mixture was stirred at room temperature overnight. The solvent was evaporated, and the residue was partitioned between ethyl acetate and 1N-hydrochloric acid solution, and washed successively with water and brine. After drying over anhydrous magnesium sulfate, the residue was purified by silica gel column chromatography to give the title compound (13.1 g, 0.047 mol, 90%).

Workup

  1. stirringthe mixture was stirred at room temperature overnight
  2. customThe solvent was evaporated
  3. customthe residue was partitioned between ethyl acetate and 1N-hydrochloric acid solution
  4. washwashed successively with water and brine
  5. dry with materialAfter drying over anhydrous magnesium sulfate
  6. customthe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-d9d61974ebe8447ca6d941525a322a59
Source dataset
uspto-grants-2015_05
Patent number
US09024044B2

Reaction notes

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