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Methyl formate → Ethyl 4-tert-butyl-5-chloro-2-ethoxybenzoate

HRID 2425588
Notes
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Reaction equation

HRID 2425588 reaction equation
[C:1]([C:5]1[C:10]([Cl:11])=[CH:9][C:8](I)=[C:7]([O:13][CH2:14][CH3:15])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:16][O-].[Na+].[CH3:19][O:20][CH:21]=[O:22]>O1CCOCC1>[C:1]([C:5]1[C:10]([Cl:11])=[CH:9][C:8]([C:21]([O:20][CH2:19][CH3:16])=[O:22])=[C:7]([O:13][CH2:14][CH3:15])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 7865Methyl formateHCID 10942334Sodium MethoxideHCID 672462864-Tert-butyl-5-chloro-2-ethoxy-1-iodobenzene

Product 1

HCID 67245813Ethyl 4-tert-butyl-5-chloro-2-ethoxybenzoateYield 80%

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent2×

Conditions

Temperature
60 °C

Procedure

To a degassed solution of 4-tert-butyl-5-chloro-2-ethoxy-1-iodobenzene (2.2 g, 6.4 mmol), sodium methoxide (0.52 g, 9.6 mmol) and dichlorobistriphenylphosphinepalladium (0.25 g, 0.4 mmol) in dioxane (20 mL) was added methylformate (1.2 mL, 19.4 mmol). The resulting mixture was heated in an oil bath (60° C.) for 18 h and then allowed to cool. The solution was diluted with dioxane and filtered through a plug of Celite and concentrated. Purification of the crude residue by flash chromatography over silica gel using 5-20% ethyl acetate in hexanes gave ethyl 4-tert-butyl-5-chloro-2-ethoxybenzoate (1.39 g, 80%) as a clear oil.

Workup

  1. temperatureto cool
  2. filtrationfiltered through a plug of Celite
  3. concentrationconcentrated
  4. customPurification of the crude residue by flash chromatography over silica gel using 5-20% ethyl acetate in hexanes

Sources & evidence

ORD record
ord-7f24652838d440f38232ada8f530c928
Source dataset
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07964724B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes