Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20039091 | HCID 20039091 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14459384 | HCID 14459384 | — |
Reaction Steps
A solution containing ethyl 4-[6,6-dimethyl-2-(1H-imidazol-1-ylmethyl)-1-heptenyl]benzoate (prepared as in Example 14; 0.7 g, 0.0017 mol) in ethanol (10 ml ) was treated with aqueous sodium hydroxide (3.5 ml of 1M). The resulting mixture was stirred at room temperature for 5 hours after which time the solvent was evaporated off under reduced pressure and the resulting residue was dissolved in water (100 ml) and washed with ethyl acetate. The aqueous solution was acidified to pH 6.5 with hydrochloric acid and extracted with ethyl acetate (3×150 ml). The extracts were combined, dried over sodium sulfate, and the solvent was evaporated off under reduced pressure to yield a crude product. The crude product was recrystallised from dichloromethane-pentane to yield 4-[6,6-dimethyl-2-(1H-imidazol-1-ylmethyl)-1E-heptenyl]benzoic acid as a colorless, crystalline solid, having a melting point of 190°-192° C. and the following structural characteristics:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04837333 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-21ab82b0a93545aeb0d6e9574fb0532d |
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| Source note | uspto-grants-1989_06 |
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