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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 28182Erstellt: 23. Oktober 2026

Diethyl Ether → Ethyl 4-nitrobenzylthioacetate

https://huagongshe.com/de/reaction/28182

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktPotassium CarbonateHCID 11430—
EduktEthyl ThioglycolateHCID 12185—
EduktBromineHCID 24408—
Edukt4-Nitrobenzyl bromideHCID 66011—
KatalysatorPotassium IodideHCID 4875—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
ProduktEthyl 4-nitrobenzylthioacetateHCID 5409246895%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04225617
Quelldatensatzuspto-grants-1980_09
ORD IDord-2faac96e9b4345a9a08a991bb9f6dca3
Quellennotizuspto-grants-1980_09