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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26813Generated: October 23, 2026

Diethyl Ether → Ethyl 4-nitrobenzylthioacetate

https://huagongshe.com/en/reaction/26813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl ThioglycolateHCID 12185—
ReactantBromineHCID 24408—
Reactant4-Nitrobenzyl bromideHCID 66011—
CatalystPotassium IodideHCID 4875—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductEthyl 4-nitrobenzylthioacetateHCID 5409246895%

Reaction Steps

43.2 g (0.2 mol) of p-nitrobenzylbromide, 200 ml of acetone, 0.2 g of potassium iodide, 24 ml of ethyl thioglycolate (namely a slight excess) and 27.6 g (0.2 mol) of potassium carbonate are successively introduced into a 1 liter 3-necked flask. The mixture is heated under reflux for about 4 hours until the bromine derivative completely disappears; the acetone is evaporated, the oil obtained is taken up in ether and in water, the ether phase is washed with a dilute solution of NaOH to remove the excess thiol, and then with a dilute solution of HCl, the solution is dried over Na2SO4 and the solvent is evaporated off. 49 g (yield: 95%) of the stated product, which is in the form of an orange coloured oil, are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04151300
Source datasetuspto-grants-1979_04
ORD IDord-3b644a4d9d3b4bcca874389de95ab514
Source noteuspto-grants-1979_04