HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 20492243, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 19438289 | HCID 19438289 | — |
| Product | HCID 20492243 | HCID 20492243 | — |
Reaction Steps
A misture of 13.0 parts of 4-dodecyloxy-2,2,6,6-tetramethylpiperidine and 3.42 parts of benzyl bromide was heated at 100° C. for 48 hours. Petroleum ether (b.p. 40°-60° C. was added to the cooled reaction mixture and the 4-dodecyloxy-2,2,6,6-tetramethylpiperidine hydrobromide formed during the reaction was filtered off. The petroleum ether solvent was removed by distillation under reduced pressure and the residue fractionally distilled to give 4-dodecyloxy-1-benzyl-2,2,6,6-tetramethylpiperidine having a boiling point of 200° C. at 0.5 m.m. of Hg. and the following elemental analysis by weight:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04049647 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-e2b62dec69ce44af987cfd1f42e00793 |
| Source note | uspto-grants-1977_09 |