HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873704Generated: October 30, 2026
HCID 86724236, compound → 3-((4-Bromo-2-iodophenoxy)methyl)-6-chlorohex-1-en-3-ol
https://huagongshe.com/reaction/873704
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86724236 | HCID 86724236 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-((4-Bromo-2-iodophenoxy)methyl)-6-chlorohex-1-en-3-ol | HCID 86724245 | — |
Reaction Steps
To a solution of 1-(4-bromo-2-iodophenoxy)-5-chloropentan-2-one (1.61 g, 3.86 mmol) in THF (35 mL) was added vinylmagnesium bromide (1M solution in THF, 4.3 mL) at −78° C. under an argon atmosphere. After stirring for 1 hour at −78° C., the mixture was gradually warmed up to −30° C. over 1 hour. The reaction was quenched by adding saturated aqueous NH4Cl solution and extracted with EtOAc. The combined organic layer were washed with brine, dried over Na2SO4, filtered, and the filtrate was evaporated. The residue was purified by silicagel column chromatography (EtOAc-hexane, a linear gradient of EtOAc from 0 to 20%) afforded 3-[(4-bromo-2-iodophenoxy)methyl]-6-chlorohex-1-en-3-ol (1.35 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08975415B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-cbd9be2fbbc74c7e8ed4bd81a35370a0 |
|---|
| Source note | uspto-grants-2015_03 |
|---|