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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647543Generated: November 1, 2026

Benzene → Ethyl 3,3-dibenzyloxypropionate

https://huagongshe.com/reaction/1647543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantBenzyl AlcoholHCID 244—
ReactantEthyl 3,3-diethoxypropionateHCID 66389—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventDiethyl EtherHCID 3283—
ProductEthyl 3,3-dibenzyloxypropionateHCID 1482590199.5%

Reaction Steps

To a 1000 mL round-bottomed flask was added ethyl 3,3-diethoxypropionate (20.0 g, 0.1051 mole), benzyl alcohol (22.7 g, 0.2102 mole), p-toluenesulfonic acid monohydrate (0.5 g, 0.0026 mole) and benzene (800 mL). The reaction can also be carried out in hexanes Heating the mixture at 80° C., the solvent was distilled from the reaction mixture in a 3.5 hour period monitored by 300 MHz NMR. The reaction can be carried out in hexanes. The resulting residue was dissolved in ether (@300 mL) and washed with saturated sodium bicarbonate solution (100 mL) and brine (100 mL). The organic layer was dried over anhydrous magnesium sulfate and the solvent removed in vacuo to give ethyl 3,3-dibenzyloxypropionate (9) as a colorless oil (32.9 g, 99.5% yield): 1H NMR (CDCl3) d 1.22 (t, 3H, J=7.2 Hz), 2.79 (d, 2H, J =5.9 Hz), 4.12 (q, 2H, J=7.2 Hz), 4.60 (d, 2H, J=11.6 Hz), 4.70 (d, 2H, J=11.6 Hz), 5.22 (t, 1H, J=6 Hz), 7.27-7.36 (m, 10H); IR (Neat) 3100, 3080, 3040, 2990, 2940, 2920, 2885, 1740, 1630, 1458, 1375, 1315, 1190, 1120, 1050, 1030, 740, 700. ##STR10##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05432273
Source datasetuspto-grants-1995_07
ORD IDord-e92c6f93bddd4de6ad0f760afbd1deae
Source noteuspto-grants-1995_07