HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 15056295, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,6-Di-tert-butyl-4-mercaptophenol | HCID 70370 | — |
| Reactant | Acryloylmorpholine | HCID 98723 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15056295 | HCID 15056295 | — |
Reaction Steps
Following the procedure of Example 4, 2,6-bis-(1,1-dimethylethyl)4-mercaptophenol (2.389, 0.01 mole) and (1-oxo-2-propenyl)morpholine (1.41 g, 0.01 mole) in methanol (75 ml) were combined with triethylamine (1.5 ml) and stirred for 12 hours at room temperature. The solvent was evaporated under a nitrogen stream leaving an orange oil which was chromatographed over silica. The product was recrystallized from a mixture of hexane, ethyl ether and methanol and the resulting white solid dried to yield the title compound, m.p. about 136.5°-137.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04959364 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-fa3f3f16320a4bb7b5ffd51c5c333b3e |
| Source note | uspto-grants-1990_09 |