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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023326Generated: October 23, 2026

Iodine → 1-[4-({[Tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]propan-2-ol

https://huagongshe.com/en/reaction/1023326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPropylene OxideHCID 6378—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromobenzyloxy-tert-butyldimethylsilaneHCID 10859583—
SolventTetrahydrofuranHCID 8028—
Product1-[4-({[Tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]propan-2-olHCID 67377030—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of (4-bromobenzyloxy)(tert-butyl)dimethylsilane (3.080 g) in THF (20 mL) were added Mg (0.288 g) and I2 (cat) at room temperature under an Ar atmosphere. The mixture was heated at 50° C. for 1 hour, and then cooled to room temperature. To the mixture was added 1,2-epoxypropane (0.77 mL) at room temperature under an Ar atmosphere, and the mixture was stirred at room temperature for 14.5 hours, and then heated at 50° C. for 1 hour, and then cooled to room temperature. To the mixture was added saturated aqueous NH4Cl, and the mixture was extracted with AcOEt. The organic layer was washed with saturated aqueous NaCl, dried over anhydrous Na2SO4, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/AcOEt=2/1) to afford 1-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]propan-2-ol (1.485 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722663B2
Source datasetuspto-grants-2014_05
ORD IDord-3bbe2a901c9b43e794b12ea9324b81fc
Source noteuspto-grants-2014_05