HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → HCID 15051991, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | HCID 14550851 | HCID 14550851 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15051991 | HCID 15051991 | 93.4% |
Reaction Steps
This compound was prepared in a manner analogous to that of Example 1, Step C, using 2.0 grams (0.0067 mole) of 2-[(4-amino-2-bromophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone and 1.0 gram (0.0067 mole) of phthalic anhydride in 50 ml of tetrahydrofuran. The reaction mixture was concentrated under reduced pressure to a residual solid. The solid was recrystallized from ethyl acetate-hexane to yield 2.8 grams of 2-[[2-bromo-4-[(2-carboxyphenyl)carbonylamino]phenyl]methyl]-4,4-dimethyl-3-isoxazolidinone, m.p. 177° C., dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892578 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-9ad1fa9b11b5463faceac04003d4414d |
| Source note | uspto-grants-1990_01 |