HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 20396662, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 20396656 | HCID 20396656 | — |
| Reactant | HCID 21822430 | HCID 21822430 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 20396662 | HCID 20396662 | — |
Reaction Steps
4-(2,2-Dimethoxyethoxy)phenol (0.05 mole), N-allyl-N-benzylcarbamoyl chloride (0.08 mole), triethylamine (0.05 mole) and xylene (50 ml) are charged into a glass reaction flask equipped with a mechanical stirrer, thermometer and reflux condenser. The mixture is stirred and heated at reflux for a period of about 12 hours. After this time the reaction mixture is cooled to room temperature and is filtered. The filtrate is then washed with water and dried over anhydrous magnesium sulfate. The dried solution is then filtered and stripped of solvent and unreacted starting materials to yield the desired product O-[4-(2,2-dimethoxyethoxy)phenyl] N-allyl-N-benzylcarbamate as the residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04163112 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-7d2d49d39e014b5c82f72a55f4407e0b |
| Source note | uspto-grants-1979_07 |