HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245475Generated: October 30, 2026
Sodium Carbonate → Carbamic acid, (4-(4-formylphenyl)-2-pyridinyl)-, 1,1-dimethylethyl ester
https://huagongshe.com/reaction/1245475
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Formylphenylboronic Acid | HCID 591073 | — |
| Reactant | (4-Iodo-Pyridin-2-Yl)-Carbamic Acid Tert-Butyl Ester | HCID 11484026 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Carbamic acid, (4-(4-formylphenyl)-2-pyridinyl)-, 1,1-dimethylethyl ester | HCID 21912851 | — |
Reaction Steps
Tetrakis(triphenylphosphine)palladium(0) (90 mg, 0.08 mmol, 0.05 equiv) was added to a deoxygenated mixture of tert-butyl 4-iodopyridin-2-ylcarbamate (1-1, 0.500 g, 1.56 mmol, 1 equiv), 4-formylphenyl boronic acid (351 mg, 2.34 mmol, 1.50 equiv), and aqueous saturated sodium carbonate solution (2.0 M, 2.3 mL, 4.7 mmol, 3.0 equiv) in dioxane (15 mL), and the resulting mixture was heated at reflux for 18 h. The reaction mixture was cooled then concentrated. The residue was partitioned between half-saturated aqueous NaCl solution (100 mL) and EtOAc (100 mL). The organic layer was dried over sodium sulfate, and concentrated to give tert-butyl 4-(4-formylphenyl)pyridin-2-ylcarbamate (2-1) as an off-white solid. LRMS m/z (M+H) Calcd: 242.2 (minus t-Bu), 199.2 (minus Boc); found 243.0 and 199.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07125888B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-6745573145bb4ac7be1e9bf674f2a298 |
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| Source note | uspto-grants-2006_10 |
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