Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | Methyl 3-oxoheptanoate | HCID 546075 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | HCID 10794130 | HCID 10794130 | — |
| Reactant | 5-[4-(Bromomethyl)[1,1′-biphenyl]-2-yl]-1-(triphenylmethyl)-1H-tetrazole | HCID 18936121 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178441886 | HCID 178441886 | — |
Reaction Steps
methyl 3-oxo-2-[[2'-(1-triphenylmethyl-1H-tetrazol-5yl)[1,1'-biphenyl]-4-yl]methyl]heptanoate. To a solution of 0.97 g of potassium 1,1-dimethylethylate in 15 ml of dimethylformamide, chilled on an ice bath, under an atmosphere of argon, a solution of 1.3 g of methyl 3-oxoheptanoate in 13 ml of dimethylformamide is added, followed by 1.67 g of lithium bromide and a solution of 5 g of 5-[4-(bromomethyl)[1,1'-biphenyl]-2-yl]-1-triphenylmethyl-1H-tetrazole in 25 ml of dimethylformamide. The reaction mixture is stirred for 5 hours at room temperature and then diluted with 300 ml of ether. The mixture is washed twice with 100 ml of water and then with 100 ml of a saturated aqueous solution of ammonium chloride. It is dried on magnesium sulfate and evaporated in vacuo to obtain 4.6 g of the product in the form of a yellow oil used as such in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05472967 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-841dc951d2dc42d09fdb00334eaf7c5c |
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| Source note | uspto-grants-1995_12 |
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