HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → O-Ethyl (3-Chlorophenyl)-thiocarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | 3-Chlorophenyl isothiocyanate | HCID 75449 | — |
| Product | O-Ethyl (3-Chlorophenyl)-thiocarbamate | HCID 54084842 | — |
Reaction Steps
A mixture of 45.5 gm (0.268 mol) of 3-chlorophenylisothiocyanate, 200 ml of anhydrous ethanol and 1 ml of quinoline was refluxed for 48 hours. Then, the reaction mixture was evaporated in an aspirator vacuum, the residue was taken up in ether, and the resulting solution was washed first with 5% hydrochloric acid and then thoroughly with water, dried, and evaporated again. After recrystallization from methanol/water, 49.5 gm (86% of theory) of colorless crystals with a melting point of 78°-79° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04353919 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-0314404d9a3246f4a990bc889874e10e |
| Source note | uspto-grants-1982_10 |