HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allylamine → HCID 57519122, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | HCID 57519121 | HCID 57519121 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57519122 | HCID 57519122 | 72% |
Reaction Steps
To a solution of 4-[1-bromo-3-(t-butyl-diphenyl-silanyloxy)-1-hydroxy-propyl]-3-vinyl-phenyl dimethylcarbamate (2.62 g, 4.62 mmol) synthesized in step (g) of Example 192 in acetonitrile (20 ml) was added allylamine (1.87 ml, 25.0 mmol) at room temperature, and the resulting mixture was stirred at room temperature overnight under a nitrogen atmosphere. After stirring, the reaction mixture was evaporated in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of hexane and ethyl acetate (2:1-0:1) as the eluent to afford the title compound (1.82 g, yield: 72%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07514475B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-d7c133479faf477193125de6ed54c061 |
| Source note | uspto-grants-2009_04 |