HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 20248673, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | N-[2-(4-aminoanilino)ethyl]methanesulfonamide; sulfuric acid | HCID 458930 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20248673 | HCID 20248673 | — |
Reaction Steps
0.2 mol (25.2 g) of sodium sulphite is added, at ambient temperature, to a solution of 0.1 mol (32.7 g) of N-(β-mesylaminoethyl)-para-phenylenediamine sulphate in 150 ml of water, and 0.13 mol (13.17 g) of acetic anhydride is added gradually, whilst stirring. When the addition is complete, stirring is continued for one hour and the expected acetylated derivative which has precipitated in crystalline form is then filtered off. The product is drained, washed with water and dried in vacuo. After recrystallisation from alcohol and drying in vacuo, it melts at 130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04295848 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-eeefe92c406c44e98bdbe8f2962e95e7 |
| Source note | uspto-grants-1981_10 |