HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170458Generated: October 29, 2026
Sodium Carbonate → Tert-butyl 2-chloro-4-(prop-1-en-2-yl)benzoate
https://huagongshe.com/reaction/2170458
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane | HCID 10997426 | — |
| Reactant | tert-Butyl 4-bromo-2-chlorobenzoate | HCID 26967600 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Tert-butyl 2-chloro-4-(prop-1-en-2-yl)benzoate | HCID 89580914 | 92.3% |
Reaction Steps
To a solution of tert-butyl 4-bromo-2-chlorobenzoate (1.0 g, 3.43 mmol) and 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (588 mg, 3.50 mmol) in 1,4-dioxane (40 mL) and water (10 mL) were added sodium carbonate (742 mg, 7.0 mmol) and tetrakis(triphenylphosphine)palladium (40 mg, 0.035 mmol). The resultant reaction mixture was stirred at 90° C. overnight under nitrogen atmosphere. After being cooled to room temperature, the reaction mixture was concentrated. The residue was purified by pre-HPLC to get tert-butyl 2-chloro-4-(prop-1-en-2-yl)benzoate (800 mg, 92.3%) as a yellow oil. LRMS (M+H+) m/z: calcd 253.09. found 253.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051269B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-2c513aa3254643a0a585c5fc1b9a2106 |
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| Source note | uspto-grants-2015_06 |
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