HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanuric chloride → 2,4-Dichloro-6-(2,2,6,6-tetramethyl-4-benzoyloxy-piperidin-1-yl)-1,3,5-triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | 2,2,6,6-Tetramethyl-4-piperidyl benzoate | HCID 579967 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2,4-Dichloro-6-(2,2,6,6-tetramethyl-4-benzoyloxy-piperidin-1-yl)-1,3,5-triazine | HCID 19991752 | — |
Reaction Steps
46.1 g of cyanuric chloride and 136.0 g of 2,2,6,6-tetramethyl-4-benzoyloxypiperidine are reacted in 300 ml of xylene as described in Example 1 and worked up. After recrystallization from isopropanol, 2,4-dichloro-6-(2,2,6,6-tetramethyl-4-benzoyloxy-piperidin-1-yl)-1,3,5-triazine are obtained as colorless crystals having a melting point of 145°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05059689 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-9ec55a07da2b40dba42ea0dc185e7fc7 |
| Source note | uspto-grants-1991_10 |