HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromide ion → HCID 66856884, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 66857182 | HCID 66857182 | — |
| Product | HCID 66856884 | HCID 66856884 | — |
Reaction Steps
To a solution of [1-(4-bromo-phenyl)-ethyl]-(4-methyl-3-oxo-pentyl)-carbamic acid methyl ester (1.78 g, 5 mmol) in dried THF (20 mL) was added allymagnesium bromide (1 M, 25 mL, 25 mmol) dropwise at −78° C. The mixture was stirred overnight. The reaction was quenched with aqueous sat. NH4Cl. The mixture was extracted with EtOAc. The organic phase was dried over Na2SO4, and condensed to give 3-{2-[1-(4-bromo-phenyl)-ethylamino]-ethyl}-2-methyl-hex-5-en-3-ol (2.2 g, crude).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575156B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-332d5f8d2f534f0cb947a939581d8c4e |
| Source note | uspto-grants-2013_11 |