Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 58780925 | HCID 58780925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 58780900 | HCID 58780900 | — |
Reaction Steps
3-Hydroxy-5-(2-methylbenzyloxy) benzoic acid (20.30 g, 78.6 mM) and acetic anhydride (125 ml, 1.32M) in acetic acid (125 ml) were refluxed for 16 hours. The reaction was cooled and the solvent evaporated ‘in vacuo’. Acetic acid (125 nml) and water (125 ml) were added to the resulting residue and the mixture was stirred for 1 hour at 50° C. Toluene (100 ml) was added and the solvent distilled off ‘in vacuo’ to give 3-acetoxy-5-(2-methylbenzyloxy) benzoic acid as a colourless solid (23.6 g); H1 NMR δ (d6-DMSO) 2.25 (3H s) 2.32 (3H s) 5.12 (2H s) 7.09–7.25 (7H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07160906B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-bdb1efd5f3b14de8a0d00d011265b3f4 |
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| Source note | uspto-grants-2007_01 |
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