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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204037Generated: October 31, 2026

Iodine → 18-(Benzyloxy)octadecan-9-ol

https://huagongshe.com/reaction/2204037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTetrahydrofuranHCID 8028—
Reactant1-BromooctaneHCID 8140—
Reactant(((10-Bromodecyl)oxy)methyl)benzeneHCID 13478286—
Product18-(Benzyloxy)octadecan-9-olHCID 86691652—

Reaction Steps

To a stirred suspension of Mg metal (0.65 g, 26.83 mmol) and a catalytic amount of Iodine in dry THF (20 ml) at 70° C., 1-bromooctane (3.57 ml, 23.48 mmol) in THF (10 ml) was added dropwise. Stirring was continued for another 30 minutes at this temperature, then the reaction mixture was cooled to room temperature, and was added slowly to a stirred solution of (((10-bromodecyl)oxy)methyl)benzene (4.4 g, 16.77 mmol) in THF (30 ml) at 0° C. The reaction was warmed to room temperature and stirring was continued for another 2 h. The reaction was quenched with ammonium chloride solution, extracted with EtOAc (3×50 ml), the combined organic layers were washed with brine solution, dried over MgSO4 and concentrated. The crude product was purified by silica gel column (12% EtOAc in Hexane) to give 18-(benzyloxy)octadecan-9-ol as a low melting white colored solid (3.85 g, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365597B2
Source datasetuspto-grants-2016_06
ORD IDord-90b75d40121142649a757e88d7cf6472
Source noteuspto-grants-2016_06