Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605573Generated: October 26, 2026

Benzyl Bromide → Benzyl 6-heptenoate

https://huagongshe.com/reaction/605573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTriethylamineHCID 8471—
Reactant6-Heptenoic acidHCID 70705—
CatalystTetrabutylammonium IodideHCID 67553—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 6-heptenoateHCID 14741231—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 6-heptenoic acid (4.71 g, 36.75 mmol) in AcOEt (80 mL) at 0° C. were successively added triethylamine (15.3 mL, 110.24 mmol), benzyl bromide (13.1 mL, 110.24 mmol) and Bu4NI (6.79 g, 18.37 mmol). The reaction mixture was stirred at 0° C. for 2H and concentrated in vacuo. The residue is taken up in AcOEt, the organic phase was washed with a saturated aqueous NaHCO3 and H2O. The organic phase was dried over MgSO4 and the solvent removed in vacuo. Flash chromatography of the residue on silica gel (n-heptane/EtOAc, 9:1) provided compound C-9 (6.00 g 75%) as a colorless oil. 13C-NMR (62.89 MHz, CDCl3): 24.42, 28.34, 33.37, 34.13, 66.08, 114.73, 128.19, 128.55, 136.16, 138.37, 173.43.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915240B2
Source datasetuspto-grants-2011_03
ORD IDord-6db620ee6cfe4d1fa9f80f861b1d3444
Source noteuspto-grants-2011_03