Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53892090 | HCID 53892090 | — |
Reaction Steps
4-(41-Hydroxyphenyl)benzoic acid (2.0 g) was dissolved in N,N-dimethylformamide (30 ml). To the solution were added benzyl bromide (3.99 g) and potassium carbonate (3.86 g). The mixture was stirred for 3 hours at 80° C. The reactiontmixture was poured into water (100 ml), which was subjected to extraction with ethyl acetate (150 ml). The organic layer was washed with 5% potassium hydrogensulfate, which was then washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off to leave 4-(4′-benzyloxyphenyl)-benzoic acid benzyl ester as a scale-like crystalline product (3.4 g). m.p.: 138-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06352982B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-ce1aafaf53a841b99baf5b6660cf85dc |
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| Source note | uspto-grants-2002_03 |
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