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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693216Generated: November 1, 2026

Benzyl Bromide → HCID 57827270, compound

https://huagongshe.com/reaction/1693216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 57827354HCID 57827354—
CatalystTetrabutylammonium IodideHCID 67553—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 57827270HCID 57827270—

Reaction Steps

DMF (40 mL) and benzyl bromide (2.4 mL, specific gravity: 1.44 g/cm3) were added to 1,1-diethoxyhept-6-en-3-ol obtained in Preparation Example 57-(1) (3.71 g), and the mixture was cooled in an ice bath under a nitrogen atmosphere. Then, sodium hydride (60%, 883 mg) was added, followed by stirring for 60 minutes. Benzyl bromide (1.09 mL) was further added, followed by stirring for one hour. Sodium hydride (60%, 116 mg) was further added, and the mixture was stirred for one hour and 50 minutes while gradually warming to room temperature. Tetrabutylammonium iodide (680 mg) was further added, followed by stirring for one hour and 10 minutes. Water and a saturated ammonium chloride solution were slowly added. After stirring for a while, the aqueous layer was separated. The organic layer was sequentially washed with a saturated ammonium chloride solution, water and brine. The resulting organic layer was dried over anhydrous magnesium sulfate. The drying agent was removed by filtration and then the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound (4.06 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158620B2
Source datasetuspto-grants-2012_04
ORD IDord-9fd1d2dbbc3849b18b7d3be70b11912d
Source noteuspto-grants-2012_04