HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → HCID 20523556, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | 1-Phenylpyrrole | HCID 12480 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 20523556 | HCID 20523556 | — |
Reaction Steps
To a mixture of 2.96 g (0.02 mole) of phthalic anhydride and 5.72 g (0.04 mole) of N-phenylpyrrole in 50 ml of chlorobenzene, maintained at 0°-5° C. in an ice bath, 810 g (0.06 mole) of aluminum chloride was added in small portions. The reaction mixture was held at 0°-5° C. for approximately two hours. The reaction was allowed to warm to room temperature and then set aside overnight at ambient temperature. The reaction mixture was worked up in a manner similar to that described in part A of Example 15 to obtain 2-[(1-phenyl-2-pyrrolyl)carbonyl]benzoic acid (Formula IX: R0 =R1 =R2 =R3 =H; R7 =C6H5) which melted over the range 159°-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04351768 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-54c1e07d51694230a03ab3015d7d702b |
| Source note | uspto-grants-1982_09 |