HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425588Generated: October 28, 2026
Methyl formate → Ethyl 4-tert-butyl-5-chloro-2-ethoxybenzoate
https://huagongshe.com/reaction/2425588
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl formate | HCID 7865 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-Tert-butyl-5-chloro-2-ethoxy-1-iodobenzene | HCID 67246286 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 4-tert-butyl-5-chloro-2-ethoxybenzoate | HCID 67245813 | 80% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964724B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-7f24652838d440f38232ada8f530c928 |
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| Source note | uspto-grants-2011_06 |
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