HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5,6,7,8-Tetrahydroquinoline-8-carbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium amide | HCID 24532 | — |
| Reactant | 5,6,7,8-Tetrahydroquinoline | HCID 66335 | — |
| Reactant | Silyl isothiocyanate | HCID 139732 | — |
| Reactant | HCID 178506835 | HCID 178506835 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5,6,7,8-Tetrahydroquinoline-8-carbothioamide | HCID 12278212 | — |
Reaction Steps
A 5,6,7,8-tetrahydroquinoline (0.01 mole) in the solvent indicated (approx. 15 ml) at 0° C. under nitrogen was treated with an alkyl lithium or a lithium amide (0.01 mole). To this solution of the 5,6,7,8-tetrahydro-8-lithioquinoline was added, at around 0° C. under nitrogen, the silyl isothiocyanate (0.01 mole) and the mixture was stirred 15 minutes. H2O (10 ml) and 2N HCl (15 ml) were added and the acid layer was separated and washed with ethyl acetate. The aqueous solution was basified (Na2CO3) and extracted with chloroform. The chloroform extracts were dried (MgSO4) and evaporated to give the 5,6,7,8-tetrahydroquinoline-8-thiocarboxamide. In this manner the thioamides in the table were prepared.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04539406 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-761dbe1bd0824287872a0f56aeaa2a36 |
| Source note | uspto-grants-1985_09 |