HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257550Generated: October 27, 2026
Cesium carbonate → Tert-butyl 4'-methyl-5-(5-oxa-6-azaspiro[3.4]oct-6-en-7-yl)biphenyl-3-carboxylate
https://huagongshe.com/reaction/1257550
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Tolylboronic acid | HCID 79799 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tert-butyl 3-bromo-5-(5-oxa-6-azaspiro[3.4]oct-6-en-7-yl)benzoate | HCID 58096138 | — |
| Catalyst | CID 53485975 | HCID 53485975 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4'-methyl-5-(5-oxa-6-azaspiro[3.4]oct-6-en-7-yl)biphenyl-3-carboxylate | HCID 66895976 | 90% |
Reaction Steps
To a solution of tert-butyl 3-bromo-5-(5-oxa-6-azaspiro[3.4]oct-6-en-7-yl)benzoate (1.36 g, 3.71 mmol) in THF (8 mL) and water (8 mL) were added (4-methylphenyl)boronic acid (1.01 g, 7.43 mmol), dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (82 mg, 0.11 mmol) and cesium carbonate (3.63 g, 11.1 mmol). The mixture was heated to 120° C. in a microwave reactor for 10 min. The mixture was cooled to ambient temperature and saturated aqueous NaHCO3 was added and the mixture was extracted with ethyl acetate (3×). The combined organic extracts were washed with water (2×), brine, dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% hexanes 85% hexanes/ethyl acetate) gave the title compound (1.26 g). MS 378.3 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461185B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-78921ca86f4b44288516dffc2e7b3b40 |
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| Source note | uspto-grants-2013_06 |
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