Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 19434486 | HCID 19434486 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178441672 | HCID 178441672 | 70% |
Reaction Steps
A mixture of 450 mg of 2-butyl-5-[(2-carboxyphenyl)methoxymethyl]-4-chloro-1-[[2'-(1-triphenylmethyltetrazol-5-yl)-1,1'-biphenyl-4-yl]methyl]-1H-imidazole, 7.5 ml of acetic acid, 3.7 ml of H2O and 2 ml of THF is stirred at room temperature for 10 hours. The solvent s are evaporated off under reduced pressure and the residue is taken up in H2O, alkalinized with 10% NaOH, an insoluble part is filtered off, the resulting solution is extracted with ether and acidified to pH 4.5 with 5N HCl. The obtained precipitate is filtered and washed with H2O. 0.2 g of a white solid are obtained (70% yield). M.p. 109°-111° C. 1H NMR (CDCl3), δ: 0.84 (t, 3 H); 1.27 (m, 2 H); 1.54 (m, 2 H); 2.39 (t, 2 H); 4.43 (s, 2 H); 4.60 (s, 2 H); 5.14 (s, 2 H); 6.80-8.12 (m, 12 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05538987 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-74815852b90a4aab9020e2557691833f |
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| Source note | uspto-grants-1996_07 |
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