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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86724236HCID 86724236—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
Product3-((4-Bromo-2-iodophenoxy)methyl)-6-chlorohex-1-en-3-olHCID 86724245—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975415B2
Source datasetuspto-grants-2015_03
ORD IDord-cbd9be2fbbc74c7e8ed4bd81a35370a0
Source noteuspto-grants-2015_03