HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlororesorcinol → 2-(5-Chloro-2,4-dihydroxybenzoyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlororesorcinol | HCID 1731 | — |
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | 2-(5-Chloro-2,4-dihydroxybenzoyl)benzoic acid | HCID 22223345 | — |
Reaction Steps
AlCl3 (40.0 g, 300 mmol) was added to a solution of phthalic anhydride (20.0 g, 135 mmol) and 4-chlororesorcinol (18.8 g, 130 mmol) in 225 ml nitrobenzene and purged with N2. After stirring overnight, the solution was poured into a vigorously stirred biphasic solution of 750 ml hexanes and 1.0 L 0.5 M aqueous HCl. The solution was allowed to stir for 2 h and the light tan precipitate that formed was filtered and washed with 200 ml aqueous 0.1 M HCl and 300 ml hexanes. The crude product was crystallized from hot MeOH/H2O (12.1 g, 32%). 1H NMR (CD3OD) δ 6.48 (1H, s), 6.95 (1H, s), 7.39 (1H, dd, J=7.2 1.5), 7.62–7.52 (2H, m), 8.12 (1H, dd, J=1.2, 7.8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07160732B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-52c1e09f42cd4d7b8d4c76b93f174c3e |
| Source note | uspto-grants-2007_01 |