HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235593Generated: October 29, 2026
Ethyl Acetate → Methyl 4-tert-butyl-3-(prop-1-en-2-yl)benzoate
https://huagongshe.com/reaction/2235593
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane | HCID 10997426 | — |
| Reactant | Methyl 3-bromo-4-(tert-butyl)benzoate | HCID 11959028 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | Methyl 4-tert-butyl-3-(prop-1-en-2-yl)benzoate | HCID 59300653 | 88% |
Reaction Steps
Methyl 3-bromo-4-tert-butylbenzoate (500 mg, 1.80 mmol, prepared according to the procedure of Hambley T. W. et al. Aust. J. Chem., 1990, 43, 807-814) and commercially available isopropenylboronic acid pinacol ester (0.693 mL, 3.6 mmol) were suspended in toluene (7 mL). Potassium carbonate (765 mg, 5.5 mmol) was added followed by Pd(PPh3)4 (213 mg, 0.180 mmol). The resulting mixture was heated to 100° C. and stirred for 24 hours. After cooling to room temperature, the mixture was treated with EtOAc (5 mL) and brine (5 mL). The organic layer was separated, washed twice with brine, dried with MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (0-10% EtOAc/hexane) to give 26.2 (378 mg, 88%) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07714008B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-22ab0369a2e74493a1ddcccfa469abd2 |
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| Source note | uspto-grants-2010_05 |
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