Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | HCID 67304495 | HCID 67304495 | — |
| Catalyst | Silver(II) oxide | HCID 92152 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 67305114 | HCID 67305114 | 82.1% |
Reaction Steps
58 μl (0.70 mmol) of allyl bromide are added to a mixture of 162 mg (0.70 mmol) of silver oxide and 200 mg (0.47 mmol) of methyl (S)-3-[3′-(3-heptyl-1-methylureido)biphenyl-4-yl]-2-hydroxypropanoate in 3 ml of diethyl ether. The reaction mixture is stirred at 40° C. for 24 hours. The mixture is filtered and then the solvents are evaporated. The residue is chromatographed on silica gel (heptane/ethyl acetate 80/20 up to 60/40). 180 mg of methyl (S)-2-allyloxy-3-[3′-(3-heptyl-1-methylureido)biphenyl-4-yl]propanoate are obtained in the form of an oil. Yield=82%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07973063B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-444469678ffd4e8d9b05c1a3116e67fd |
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| Source note | uspto-grants-2011_07 |
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