HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906154Generated: October 27, 2026
Cesium carbonate → (R)-methyl 5-(sec-butylamino)-4-cyano-2-methylbenzoate
https://huagongshe.com/reaction/906154
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | (R)-sec-butylamine | HCID 2724537 | — |
| Reactant | Methyl 4-cyano-5-iodo-2-methylbenzoate | HCID 67402433 | — |
| Reactant | Bis(diphenylphosphino)xanthene | HCID 86631950 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (R)-methyl 5-(sec-butylamino)-4-cyano-2-methylbenzoate | HCID 67404849 | 73.4% |
Reaction Steps
To a solution of methyl 4-cyano-5-iodo-2-methylbenzoate (500 mg, 1.66 mmol) in 1,4-dioxane (25 mL) was added 9,9-dimethyl-4,5-(bis(diphenylphosphino)xanthene (96 mg, 0.166 mmol), tris(dibenzylideneacetone)-dipalladium (76 mg, 0.083 mmol), cesium carbonate (1.08 g, 3.32 mmol) and (R)-butan-2-amine (506 μL, 4.98 mmol). The reaction mixture was heated to 95° C. and stirred for 16 h, at which time it was cooled to room temperature. The heterogeneous mixture was filtered through a bed of celite, and the filter cake rinsed with ethyl acetate. The filtrate was concentrated, and the residue was purified by flash chromatography (100% hexanes to 5% ethyl acetate in hexanes) to afford (R)-methyl 5-(sec-butylamino)-4-cyano-2-methylbenzoate (300 mg, 73%) as a bright yellow oil. MS (EI) for C14H18N2O2: 247 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012956B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-56f4bd5e5abc4c9cb6205e213034de88 |
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| Source note | uspto-grants-2011_09 |
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