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Benzyl Bromide → HCID 11759308, compound

HRID 1826072
Notes
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Reaction equation

HRID 1826072 reaction equation
[CH3:1][S:2][CH:3]([C:7]1[CH:12]=[C:11]([CH:13]=[O:14])[CH:10]=[CH:9][C:8]=1[O:15][CH3:16])[C:4]([OH:6])=[O:5].C(=O)([O-])[O-].[K+].[K+].[CH2:23](Br)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>CN(C)C=O>[CH3:1][S:2][CH:3]([C:7]1[CH:12]=[C:11]([CH:13]=[O:14])[CH:10]=[CH:9][C:8]=1[O:15][CH3:16])[C:4]([O:6][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:5]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 12017994HCID 12017994, compound

Product 1

HCID 11759308HCID 11759308, compoundYield 83%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

Ethyl 2-methylthio-2-(5-formyl-2-methoxyphenyl)acetate (4.80 g, 17.9 mmol), ethanol (30 mL) and 10% aqueous solution of sodium hydroxide (20 mL) were mixed and the mixture was stirred for 3 hours at room temperature. The reaction mixture was poured in ice water and made acidic with concentrated hydrochloric acid, which was then extracted with ethyl acetate. The extracte was washed with water, dried over anhydrous sodium sulfate, and then concentrated to afford 4.00 g of crude 2-methylthio-2-(5-formyl-2-methoxyphenyl)acetic acid as yellow crystals (this compound was used for next reaction without further purification). Next, 2-methylthio-2-(5-formyl-2-methoxyphenyl)acetic acid (4.00 g, 16.4 mmol) and N,N-dimethylformamide (50 mL) were mixed and, after anhydrous potassium carbonate (3.71 g, 26.8 mmol) and benzyl bromide (3.06 g, 17.9 mmol) were added at room temperature under stirring, the mixture was stirred for 5 hours. The reaction mixture was poured in ice water and extracted with ether. The extracted solution was washed with water and brine, and then dried over anhydrous sodium sulfate. The reaction mixture was concentrated and the residue was purified by silica gel column chromatography (eluate n-hexane:ethyl acetate=6:1 v/v) to afford 4.50 g (76%) of the title compound as a light brown oil.

Workup

  1. customwas used for next reaction without further purification)
  2. stirringthe mixture was stirred for 5 hours
  3. extractionextracted with ether
  4. washThe extracted solution was washed with water and brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationThe reaction mixture was concentrated
  7. customthe residue was purified by silica gel column chromatography (eluate n-hexane:ethyl acetate=6:1 v/v)

Sources & evidence

ORD record
ord-d796823bfc4f4e9f90625958e7355b5f
Source dataset
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07049342B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes