HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869018Generated: October 30, 2026
Ethyl 2-iodo-3-methylbenzoate → Ethyl 3-methyl-2-(oxazol-2-yl)benzoate
https://huagongshe.com/reaction/869018
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-iodo-3-methylbenzoate | HCID 12140519 | — |
| Reactant | 2-(Tri-n-butylstannyl)oxazole | HCID 15486183 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Ethyl 3-methyl-2-(oxazol-2-yl)benzoate | HCID 90412267 | 2,057.2% |
Reaction Steps
In a microwave vial was dissolved ethyl 2-iodo-3-methylbenzoate (627 mg, 2.16 mmol) and 2-(tributylstannyl)oxazole (0.54 mL, 0.07 mmol) in DME (2.59 mL). The solution was degassed with N2 for 5 minutes then CuI (21 mg, 0.11 mmol) and Pd(PPh3)4 (125 mg, 0.11 mmol) were added. The reaction was purged with N2 and heated at 150° C. for 1 h. The reaction was cooled to room temperature, filtered through a pad of Celite and purified via silica gel chromatography (0-40% EtOAc in hexanes) to give the title compound of step A (333 mg, 67%). MS (ESI) mass calcd. for C13H13NO3, 231.1. m/z found 232.1 [M+H]+. 1H NMR (500 MHz, Chloroform-d) δ 7.89-7.82 (m, 1H), 7.79 (d, J=0.8 Hz, 1H), 7.48-7.43 (m, 2H), 7.30 (d, J=0.9 Hz, 1H), 4.17 (q, J=7.1 Hz, 2H), 2.27 (s, 3H), 1.18 (t, J=7.1 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969352B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-36d9eb1fda7f411eb216a2a6997beb0e |
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| Source note | uspto-grants-2015_03 |
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