HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53009Generated: October 28, 2026
Sodium ethoxide → HCID 19036262, compound
https://huagongshe.com/reaction/53009
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 19036200 | HCID 19036200 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19036262 | HCID 19036262 | 92.2% |
Reaction Steps
0.75 ml of a 0.15N solution of sodium ethoxide in ethanol was added to a solution of 1.69 g of ethyl 2-acetoxymethyl-4-(1-hydroxy-1-methylethyl)-1-{4-[2-(trityltetrazol-5-yl)phenyl]phenyl}methylimidazole-5-carboxylate [prepared as described in Example 102(a)] in 15 ml of ethanol, and the mixture was stirred at room temperature for 5 minutes. The reaction solution was then concentrated by evaporation under reduced pressure, ethyl acetate and water were added to the residue, and the ethyl acetate layer was separated. This ethyl acetate layer was washed with an aqueous solution of sodium chloride and then dried over anhydrous sodium sulfate, after which it was concentrated by evaporation under reduced pressure. The resulting residue was purified by recrystallization from a mixture of diethyl ether and diisopropyl ether, to give 1.47 g of the title compound as crystals, melting at 151°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616599 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-88b6f19ea8c042c39c2d6b6b3e564a0c |
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| Source note | uspto-grants-1997_04 |
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