Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Butynoic Acid | HCID 137547 | — |
| Reactant | HCID 21250534 | HCID 21250534 | — |
| Catalyst | Chlorotris(triphenylphosphine)rhodium(I) | HCID 84599 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 16450136 | HCID 16450136 | — |
Reaction Steps
A mixture of di-prop-2-ynyl-carbamic acid tert-butyl ester (4.78 g, 24.7 mmol) and ethanol (120 mL) was prepared under argon and cooled to 0° C. for 15 min. 3-Butynoic acid (3.64 g, 43.3 mmol) and tris(triphenylphosphine)rhodium (I) chloride (1.14 g, 1.23 mmol) were added and reaction was gradually warmed to room temperature over 1.3 hr. The reaction was then heated to 45° C. for 17 hr. The reaction was cooled to room temperature and concentrated in vacuo. The residue was diluted with 1N NaOH and extracted with diethyl ether (3×). The aqueous layer was acidified to pH˜1 with 1N HCl and extracted with EtOAc (3×). The combined EtOAc layers were dried over Na2SO4, filtered, and concentrated. The crude product was purified by flash chromatography on silica gel (EtOAc:Hexane, 5-100%). ESI-MS m/z 278 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376454B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-c9fee07b185c494b848331e4685a5ef3 |
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| Source note | uspto-grants-2016_06 |
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