HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048102Generated: October 31, 2026
Triethylamine → Methyl 5-chloro-2-fluoro-4-methylbenzoate
https://huagongshe.com/reaction/2048102
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Bromo-2-chloro-5-fluorotoluene | HCID 2736228 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 5-chloro-2-fluoro-4-methylbenzoate | HCID 58042513 | 93% |
Reaction Steps
To a solution of 1-bromo-5-chloro-2-fluoro-4-methylbenzene (10 g, 44.7 mmol) in methanol (200 mL) was added 1,1′-binaphthalene-2,2′-diylbis(diphenylphosphine)-dichloropalladium (1:1) (358 mg, 0.447 mmol) and N,N-diethylethanamine (8.11 mL, 58.2 mmol). The resulting mixture was placed in a bomb and pressurized with carbon monoxide to 80 psi and heated at 80° C. for 18 hours. The cooled reaction mixture was then concentrated in vacuo to yield a semi-solid, which was dissolved in EtOAc (300 mL) and washed with water (200 mL). The organic layer was separated, dried over magnesium sulphate, filtered and concentrated in vacuo to yield an orange oil, which solidified on standing (9.87 g). The solid was purified by silica gel column chromatography eluting with 0 to 20% EtOAc in heptane to afford the title compound as a crystalline white solid (8.47 g, 93%):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592629B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-dadb30a509f74c179e2db7411ecbdf2a |
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| Source note | uspto-grants-2013_11 |
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