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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83563Generated: October 29, 2026

Water → 1-Bromo-3-butylbenzene

https://huagongshe.com/reaction/83563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Bromobenzyl bromideHCID 69979—
ReactantHCID 178455851HCID 178455851—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-3-butylbenzeneHCID 13954102—

Reaction Conditions

Temperature0 °C

Reaction Steps

Under nitrogen stream, to a solution of 1-bromo-3-bromomethylbenzene (25 g) in tetrahydrofuran (200 ml) were sequentially added dropwise n-propylmagnesium bromide (60 ml, 2M solution in tetrahydrofuran) and lithium tetrachlorocuprate (5 ml, 0.1M solution in tetrahydrofuran) at −78° C. Then, this reaction mixture was stirred at 0° C. for 2 hours. Under ice-cooling, to this reaction mixture were sequentially added a saturated aqueous solution of ammonium chloride (100 ml) and water (100 ml), and the mixture was extracted with ethyl acetate (200 ml). The resulting aqueous layer was again extracted with ethyl acetate (100 ml), the combined organic layer was washed with a saturated aqueous solution of sodium chloride (100 ml), and dried over anhydrous sodium sulfate. This organic layer was concentrated under reduced pressure, the resulting residue was purified by silica gel chromatography (eluent: n-hexane/ethyl acetate=1/0 to 100/1) to give the titled compound (8.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846746B2
Source datasetuspto-grants-2014_09
ORD IDord-d13bbf0564d04658a888a63850f10bbb
Source noteuspto-grants-2014_09