Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Hydroxybenzyl alcohol | HCID 102 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Acetoxybenzoyl chloride | HCID 79668 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Aspirin | HCID 2244 | 200% |
Reaction Steps
3-hydroxymethylphenol (10 g, 0.08 moles) is dissolved in toluene (50 ml) containing triethylamine (9.8 g, 0.1 moles). To the so obtained solution an acetylsalicylic acid chloride solution (16 g, 0.08 moles) in toluene (50 ml) is added at a temperature of 5°-10° C. under stirring. The mixture is maintained at a temperature in the above mentioned range, under stirring for 2 hours, then poured in water and then extracted with dichloromethane (2×100 ml). The organic phase is separated, washed in sequence with a 25% w/v potassium carbonate solution, with water, with a 3% hydrochloric acid solution and lastly with water again, then anhydrified with sodium sulphate and the solvent evaporated under vacuum. The residue is crystallized from isopropanol. 3-hydroxymethylphenyl ester of the 2-acetoxybenzoic acid (45.8 g, 0.16 moles, yield 80%) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06696591B1 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-8506c41f362147718d0510ce369ea929 |
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| Source note | uspto-grants-2004_02 |
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