HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 178503572, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Methylthio-5-bromo-6-methylpyrimid-2-one | HCID 20494288 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | HCID 178503296 | HCID 178503296 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178503572 | HCID 178503572 | 28% |
Reaction Steps
4-Methylthiopyrimid-2-one (prepared as described in Wheller, L. H. and Johnson, B. T. J. Amer. Chem. Soc. 42 (1909) (30), (0.01 mol) was dissolved at ca. 80° C. in acetic acid (30 ml) containing 2% acetic anhydride. The temperature was lowered to ca. 55° C. and N-bromosuccinimide (0.013 mol) added and the reaction mixture stirred at this temperature for 40 min. Ice-cold water (150 ml) containing a little sodium bisulphite was then added and the precipitated collected and recrystallised from water; yield 28%, m.p. 260° C.;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04395406 |
| Source dataset | uspto-grants-1983_07 |
| ORD ID | ord-bc817db23ba34f979a11c43532a729f9 |
| Source note | uspto-grants-1983_07 |