Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Ethyl 3-cyclopropyl-3-oxopropanoate | HCID 262979 | — |
| Reactant | HCID 178456127 | HCID 178456127 | — |
| Product | HCID 90332535 | HCID 90332535 | 21% |
Reaction Steps
(t-BuO)2 (94 g, 640 mol) was added to a solution of ethyl 3-cyclopropyl-3-oxopropanoate (50 g, 320 mmol), 4-bromophenol (166 g, 9.6 mol) and FeCl.6H2O (5.8 g, 32 mmol) in Di-chlorine Ethane (316 g, 3.2 mol) under N2 gas at 25° C. The mixture was stirred at 80° C. for 6 hours. The solvent was removed and the residue was purified by column chromatography (eluted with PE:EA from 20:1 to 10:1) to furnish the pure product of ethyl 5-bromo-2-cyclopropylbenzofuran-3-carboxylate (20.0 g, yield: 21%). 1H-NMR (400 MHz, CDCl3) δ 8.02 (s, 1H), 7.30 (d, J=7.2 Hz, 1H), 7.18 (d, J=7.2 Hz, 1H), 4.42 (q, J=7.2 Hz, 2H), 3.01˜3.05 (m, 1H), 1.44 (t, J=7.2 Hz, 3H), 1.24˜1.26 (m, 2H), 1.16˜1.19 (m, 2H). MS (M+H)+: 309/311.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242998B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-f9a104db774b4200a6564d4917ab1d6c |
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| Source note | uspto-grants-2016_01 |
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