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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695852Generated: October 31, 2026

Triethylsilane → 6-(2-Bromo-5-iodo-benzyl)-chroman

https://huagongshe.com/reaction/1695852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
Reactant(2-Bromo-5-iodo-phenyl)-chroman-6-yl-methanoneHCID 58340801—
SolventAcetonitrile methylene chlorideHCID 21877088—
Product6-(2-Bromo-5-iodo-benzyl)-chromanHCID 5834081577.5%

Reaction Steps

To a stirred solution of (2-bromo-5-iodo-phenyl)-chroman-6-yl-methanone (2.0 g, 4.51 mmol) in acetonitrile:dichloromethane (2:1 mixture, 9 mL) was added triethylsilane (2.52 mL, 15.78 mmol) and boron trifluoride diethyl etherate complex (1.11 mL, 9.02 mmol) at 0° C. After stirring overnight at room temperature, reaction was quenched by the addition of saturated aqueous sodium bicarbonate solution. Volatiles were evaporated under reduced pressure. The aqueous layer was extracted with ethyl acetate (2×20 mL). Ethyl acetate layer was washed with water, brine, dried over sodium sulfate, concentrated and purified by silica gel column chromatography to furnish 6-(2-bromo-5-iodo-benzyl)-chroman (1.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163704B2
Source datasetuspto-grants-2012_04
ORD IDord-9e1d534442c048a9954f7d3de0960def
Source noteuspto-grants-2012_04