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Sodium bis(trimethylsilyl)amide → HCID 67044336, compound

HRID 2261962
Notes
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Reaction equation

HRID 2261962 reaction equation
[CH3:1][Si](C)(C)[N-][Si](C)(C)C.[Na+].[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]([C:20]2[CH:29]=[CH:28][CH:27]=[CH:26][C:21]=2[C:22]([O:24][CH3:25])=[O:23])=O)=[CH:14][C:13]=1[N+:30]([O-:32])=[O:31]>[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.O1CCCC1>[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]([C:20]2[CH:29]=[CH:28][CH:27]=[CH:26][C:21]=2[C:22]([O:24][CH3:25])=[O:23])=[CH2:1])=[CH:14][C:13]=1[N+:30]([O-:32])=[O:31]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 2724254Sodium bis(trimethylsilyl)amideHCID 14994660Methyl 2-(4-chloro-3-nitrobenzoyl)benzoate

Product 1

HCID 67044336HCID 67044336, compoundYield 14%

Reagents, catalysts & solvents 2

HCID 74505Methyltriphenyliphosphonium bromideCatalystHCID 8028TetrahydrofuranSolvent
2×

Conditions

Temperature
0 °C

Procedure

To a mixture of methyltriphenylphosphonium bromide (15.6 g, 44 mmol) in tetrahydrofuran (100 mL) at 0° C. was added a solution of sodium hexamethyldisilazide (22 mL, 2.0M solution in THF, 44 mmol), and the resulting mixture was stirred for one hour at 0° C. Methyl 2-[(4-chloro-3-nitrophenyl)carbonyl]benzoate (7.0 g, 22 mmol) in tetrahydrofuran (50 mL) was then added drop wise to the yellow reaction mixture and stirred at 0° C. for 30 minutes and at room temperature for four hours. The brown reaction mixture was diluted with hexanes, filtered through silica gel, and the filtrate was washed with water (100 mL), brine solution (100 mL), dried over sodium sulfate, filtered, concentrated, and purified by flash chromatography (silica gel, eluting with 5-10% ethyl acetate-hexane) to give methyl 2-[1-(4-chloro-3-nitrophenyl)ethenyl]benzoate (0.95 g, 3 mmol, 14% yield). 1H NMR (400 MHz, CDCl3): 7.95-7.93 (dd, 1H), 7.73-7.72 (d, 1H), 7.61-7.57 (dt, 1H), 7.50-7.46 (dt, 1H), 7.46-7.43 (d, 1H), 7.39-7.34 (m, 2H), 5.77 (s, 1H), 5.37 (s, 1H), 3.63 (s, 3H); MS (EI) for C16H12ClNO4: 318 (MH+).

Workup

  1. stirringstirred at 0° C. for 30 minutes and at room temperature for four hours
  2. filtrationfiltered through silica gel
  3. washthe filtrate was washed with water (100 mL), brine solution (100 mL)
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. custompurified by flash chromatography (silica gel, eluting with 5-10% ethyl acetate-hexane)

Sources & evidence

ORD record
ord-e08e9634b8cc41239b45ebb8b53b3729
Source dataset
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07846959B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes