HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methoxy-2,2,6,6-tetramethyl-piperidin-4-ol → 1-Methoxy-2,2,6,6-tetramethylpiperidin-4-yl 3-(5-Chlorobenzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methoxy-2,2,6,6-tetramethyl-piperidin-4-ol | HCID 10997770 | — |
| Reactant | 3-(5-Chlorobenzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamic acid | HCID 18008718 | — |
| Product | 1-Methoxy-2,2,6,6-tetramethylpiperidin-4-yl 3-(5-Chlorobenzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate | HCID 10187264 | — |
Reaction Steps
3-(5-Chlorobenzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamic acid (12.0 g, 0.032 mol) and 1-methoxy-2,2,6,6-tetramethyl-4-hydroxypiperidine (6.66 g, 0.036 mol) are reacted together according to the procedure given in Example 3. The title compound is obtained in a yield of 8.79 g (50.5%) as a light yellow solid, melting at 132-137° C., whose structure is consistent with 1Hnmr and mass spectrometry. The compound has a molar absorptivity of 17,210 l/mole cm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07419513B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-3d50e7e410914d55bf1150f6d833304a |
| Source note | uspto-grants-2008_09 |