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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862863Generated: October 29, 2026

Iodine → 1-(3-Bromophenyl)octan-1-ol

https://huagongshe.com/reaction/862863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1-BromoheptaneHCID 12369—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-BromobenzaldehydeHCID 76583—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Bromophenyl)octan-1-olHCID 21849174—

Reaction Conditions

Temperature65 °C

Reaction Steps

A small amount of iodine was added to a solution (100 ml) of magnesium (9.8 g) in anhydrous tetrahydrofuran and the mixture was stirred at 50° C. until the color of the iodine disappeared. A solution of heptyl bromide in anhydrous tetrahydrofuran (200 ml) was dropwise added thereto over 1 hour. The mixture was stirred at 65° C. for 1 hour and a solution of m-bromobenzaldehyde in anhydrous tetrahydrofuran (200 ml) was dropwise added thereto under ice-cooling. The mixture was stirred at room temperature for 30 minutes. Under ice-cooling, a saturated aqueous ammonium chloride solution (7.3 ml) was added thereto and the mixture was stirred for 1 hour. The insoluble matters were filtered off and the filtrate was concentrated. The concentrate was dissolved in ethyl acetate and the mixture was washed with water. The mixture was dried over magnesium sulfate and the solvent was distilled away. The residue obtained was purified by silica gel column chromatography (eluent; hexane:ethyl acetate=10:1) to give 50.9 g of the subject compound as an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719176
Source datasetuspto-grants-1998_02
ORD IDord-d77012a9c0814aa5a4af4a5d2e1b6135
Source noteuspto-grants-1998_02