Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | HCID 21150551 | HCID 21150551 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 20140932 | HCID 20140932 | — |
Reaction Steps
5 g of gaseous hydrogen chloride are introduced at -30° C. into 300 ml of dimethoxyethane, followed by the addition of 6.4 g of 1,3,5-triisopropyl-2,4,6-hexahydrotriazine. The reaction mixture is kept at -20° C., during which time 12 g of α-methylmercaptoisobutyric acid amide are added. The reaction mixture is stirred for 21/2 hours at room temperature. Then, likewise at -20° C., 50 ml of a 20% phosgene solution in toluene and, subsequently, a solution of 15 ml of pyridine in 30 ml of dimethoxyethane are added dropwise to the reaction mixture. The mixture is then stirred for 1 hour at room temperature. A further 30 ml of pyridine are then added dropwise, and the mixture is stirred for a further 4 hours at 60° C. For working up, the reaction mixture is cooled and filtered, and the filtrate is concentrated by evaporation. The residue is taken up in ethyl acetate, and the resultant solution is extracted twice with water and twice with a saturated sodium chloride solution. The separated organic phase is dried over sodium sulfate and concentrated by evaporation. The residue is taken up in hexane, a small amount of silica gel is added, and the batch is filtered. The filtrate is concentrated by evaporation, thus affording the title compound of the formula ##STR6## with a refractive index nD20 of 1.5028 (compound 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04742056 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-965bfdd760aa4326825ac1aae6c9aee9 |
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| Source note | uspto-grants-1988_05 |
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