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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628160Generated: October 29, 2026

Benzyl Bromide → HCID 86715372, compound

https://huagongshe.com/reaction/628160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Acetylthiohexanoic acid 97HCID 4604910—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 86715372HCID 8671537250%

Reaction Steps

Referring to FIG. 40, to a solution of 6-(acetylthio)hexanoic acid (3 g, 15.8 mmol) in CH3CN (80 mL) were added K2CO3 (4.3 g, 31.6 mmol) and benzyl bromide (2.68 g, 15.8 mmol). The reaction mixture was stirred at room temperature overnight and ethyl acetate (200 mL) and water (100 mL) were added. The organic layer was separated, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (2.2 g, 50% yield) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309283B2
Source datasetuspto-grants-2016_04
ORD IDord-846f881aef214fb685c32ca7a62bae5f
Source noteuspto-grants-2016_04