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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714756Generated: October 30, 2026

Benzyl Bromide → HCID 15948207, compound

https://huagongshe.com/reaction/1714756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTriethylamineHCID 8471—
ReactantHydroxycaprylic AcidHCID 94180—
CatalystTetrabutylammonium IodideHCID 67553—
SolventEthyl AcetateHCID 8857—
ProductHCID 15948207HCID 15948207—

Reaction Steps

To a solution of a commercially available racemic 2-hydroxyoctanoic acid mixture (1.00 g, 6.2 mmol.) in HPLC-grade ethylacetate (30 ml), there are added in succession benzyl bromide (2.22 ml; 18.7 mmol.), triethylamine (2.6 ml, 18.7 mmol.) and tetrabutylammonium iodide (1.15 g; 3.12 mmol.). The solution is stirred for 18 hours at room temperature and the solvent is thereafter evaporated. The residue is taken up into ether and the organic layer is then washed with a saturated solution of NaHCO3 and H2O (2×). The organic layer is dried over MgSO4, filtered and evaporated to yield crude benzyl 2-hydroxyoctanoate (Rf=0.57 in a 3/1 petroleum ether/EtOAc mixture; phosphomolybdinium compound and U.V. color development agent)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799762B2
Source datasetuspto-grants-2010_09
ORD IDord-4d76da1a69914a4b90585d47b77fba8c
Source noteuspto-grants-2010_09