Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Zinc Acetate | HCID 11192 | — |
| Reactant | 5-Phenyl-2-(trichloromethyl)-1,3-oxazolidine | HCID 23455111 | — |
| Product | HCID 21453983 | HCID 21453983 | 58% |
Reaction Steps
A mixture of 30.3 g (0.3 mole) triethylamine, 12.3 g. (0.1 mole) zinc acetate, 55.0 g. (0.206 mole) 5-phenyl-2-trichloromethyloxazolidine and 15.6 g. (0.206 mole) carbon disulfide was stirred at ambient temperatures for 17 hours and then was heated at 50° C. for three hours. A reddish amber-colored semi-solid was obtained after the volatile materials were distilled off at 50°/25 mm. Hg. The semi-solid was dissolved in methanol and the resulting solution added to water with vigorous stirring. The solids were filtered, air-dried, and redissolved in benzene. After drying the solution with magnesium sulfate, filtering the mixture and evaporating the solvent, 37 g. (58%) of the desired product (m.p. 91°-93° C.) was obtained; its infrared spectrum was consistent with the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03987017 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-05913aa632494debb4a40d873d07086c |
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| Source note | uspto-grants-1976_10 |
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