HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Disulfide → HCID 22766682, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(heptan-3-yl)-1,3-oxazolidine | HCID 287363 | — |
| Reactant | HCID 86735842 | HCID 86735842 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 22766682 | HCID 22766682 | — |
Reaction Steps
To a solution of 117 g (1.16 moles) of triethylamine and 133 g (0.77 mole) of 2-(1-ethylpentyl)oxazolidine [containing mainly the tautomer, N-α-ethylpentylidene-2-hydroxyethylamine, and prepared according to A. Cope, J.A.C.S. 64, 1503 (1942)] in one liter of ether was added 88 g (1.16 moles) of carbon disulfide at 10°-20° over a period of 35 minutes. Stirring was continued for 17 hours at ambient temperatures. Solids (13 g of triethylammonium N-(2-hydroxyethyl)dithiocarbamate were filtered off and the resulting filtrate was removed of volatiles at 25°/150 mm Hg to give 242g of crude triethylammonium 2-(1-ethylpentyl)-3-oxazolidinecarbodithioate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04118378 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-58121ca1997e40ffb6b89d55b18718ce |
| Source note | uspto-grants-1978_10 |