HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 86743121, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86743122 | HCID 86743122 | — |
| Product | HCID 86743121 | HCID 86743121 | — |
Reaction Steps
68 Parts of 4-(3'-nitro-4'-chlorobenzoyl)-amino-2,2,6,6-tetramethylpiperidine are added to 250 parts of acetic anhydride. After the addition of 21 parts of triethylamine, the suspension is stirred for 16 hours at toom temperature and then for 3 hours at 100°-110°. In order to complete precipitation of the acetyl derivative, 1500 parts by volume of cold water are added and stirred at room temperature until all the excess acetic anhydride is destroyed. The precipitate is then filtered, washed neutral with water and dried. 72 parts of 4-(3'-nitro-4'-chlorobenzoyl)-amino-1-acetyl-2,2,6,6-tetramethyl-piperidine having a melting point of 198°-200° results.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04866113 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-cae37c96478742fba79b28cd55e12e04 |
| Source note | uspto-grants-1989_09 |