Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409373Generated: October 26, 2026

Hydrochloric Acid → 2,6-Diethylbenzyl acetate

https://huagongshe.com/reaction/409373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetone cardiceHCID 18522661—
Reactant2,6-Dibromobenzyl acetateHCID 59216413—
ReactantHCID 178418750HCID 178418750—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTetrahydrofuranHCID 8028—
SolventEthylacetate heptaneHCID 21899848—
Product2,6-Diethylbenzyl acetateHCID 6674163863%

Reaction Steps

To a cooled (dry ice-acetone bath) mixture of 2,6-dibromo-benzyl acetate (5.05 g, 16.4 mmol) and PdCl2(dppf) (0.08 eq) in dry THF (50 mL) was added 1.1 M Et2Zn (60 mL, 66 mmol, 4 eq). The resulting mixture was allowed to warm to RT, stirred at 45° C. (programmed block temperature, ˜40 h), and added to a stirred mixture of dilute HCl and heptane/EtOAc. The organic layer was dried (Na2SO4), filtered, and evaporated. Chromatography (2%-10% EtOAc/heptane stepwise gradient) gave 2.12 g (yield of 63%) of the title product, along with 0.20 g of 2,6-diethylbenzyl alcohol. 1H NMR (300 MHz, CDCl3) δ 1.21 (t, 6H), 2.07 (s, 3H), 2.70 (q, 4H), 5.19 (s, 2H), 7.09 (d, 2H), 7.22 (dd, 1H). The following compound was prepared by making appropriate substitutions to the above procedure:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759340B2
Source datasetuspto-grants-2014_06
ORD IDord-9ee2dd48d44747b198a9062557002bd1
Source noteuspto-grants-2014_06