HuagongsheHuagongshe Chemistry Print Report · For research reference only
Succinic anhydride → HCID 86758459, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | p-Hydroxyaniline mustard | HCID 71000 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86758459 | HCID 86758459 | 83% |
Reaction Steps
To a suspension of succinic anhydride (225 mg, 2.25 mmol) in CHCl3 (10 ml) was added under stirring, 4-[N,N-bis(2-chloroethyl)-amino]phenol (compound 6, FIG. 7; 203 mg, 0.75 mmol) followed by triethylamine (75 mg, 0.75 mmol). The mixture was stirred overnight and the solvent evaporated. The crude residue was dissolved in EtOAC/Et2O/H2O and under stirring the pH was adjusted to 3. The organic layer was washed with water, brine, dried (MgSO4), and evaporated. The resulting oil was crystallised from Et2O/hexane and the white solid was filtered off and dried under vacuum to obtain the desired end product (210 mg; yield 83%). Melting point 98-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06436691B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-a9a030a72b8048f7a5cab87c596b41be |
| Source note | uspto-grants-2002_08 |