HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Ethyl 4-nitrobenzylthioacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 4-nitrobenzylthioacetate | HCID 54092468 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04151300 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-3b644a4d9d3b4bcca874389de95ab514 |
| Source note | uspto-grants-1979_04 |