HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → HCID 68121707, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,6-Bis(tert-butylamino)-4-methylpyridin-3-yl methyl ketone | HCID 94005 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68121707 | HCID 68121707 | — |
Reaction Steps
534 mg. (3 mmol.) of N-bromosuccinimide (recrystallized from water) were added in small portions to a solution of 831 mg. (3 mmol.) of 3-acetyl-2,6-di-t-butylamino-4-methylpyridine (Compound V) in 20 ml. of carbon tetrachloride and 5 ml. of ethanol, and the reaction mixture was allowed to stand overnight at room temperature. The reaction mixture was evaporated down at reduced pressure, and the residue was partitioned between ether and water. The organic phase was dried over anhydrous sodium sulfate and evaporated at reduced pressure to obtain yellow crystals. Recrystallization from methanol/water gave the product (990 mg.), m.p. 99°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04052510 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-722d30080ad3412a995daec9ac3fd474 |
| Source note | uspto-grants-1977_10 |