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Acetone → Benzoic acid, 2-ethoxy-4-methyl-, ethyl ester

HRID 924966
Notes
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Reaction equation

HRID 924966 reaction equation
[OH:1][C:2]1[CH:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].C([O-])([O-])=O.[K+].[K+].[CH2:18](I)[CH3:19].[CH3:21][C:22](C)=O>>[CH2:21]([O:1][C:2]1[CH:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH2:18][CH3:19])=[O:5])[CH3:22]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 180AcetoneHCID 57882-Hydroxy-p-toluic acidHCID 6340IodoethaneHCID 11430Potassium Carbonate

Product 1

HCID 11816602Benzoic acid, 2-ethoxy-4-methyl-, ethyl esterYield 85%

Procedure

To a mixture of 2-hydroxy-4-methylbenzoic acid (5.0 g, 32.9 mmol), K2CO3 (18.9 g, 136.6 mmol) and acetone (50 mL) was added ethyl iodide (41.0 g, 263.2 mmol). The mixture was stirred at room temperature for 3 days. After filtration, the organic layer was concentrated to afford ethyl 2-ethoxy-4-methylbenzoate as colorless oil (5.7 g, 85%), which was used directly for next step.

Workup

  1. filtrationAfter filtration
  2. concentrationthe organic layer was concentrated

Sources & evidence

ORD record
ord-c7d1e2c07b774c99a9e38e8a068dc098
Source dataset
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09283229B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes