Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | 2-Benzylthio-2-thiazoline | HCID 275677 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-benzyl-thiazolinethion | HCID 125489430 | 704.2% |
Reaction Steps
12.7 g (0.1 mole) of benzylchloride were added to 209.2 g (1 mole) of 2-benzylthio-thiazoline and the mixture was heated to 150° C. for eight hours. The mixture was allowed to cool down to 70° C. and 500 ml of methanol were added. The reaction mixture was allowed to cool down to room temperature and stirred for an additional hour; N-benzyl-thiazoline-thion precipitated from the medium as a white crystalline product, was isolated by filtration and washed twice with 10 ml of methanol. The crude product was recrystallized from a minimum of acetonitrile. 146 g of N-benzyl-thiazolinethion were isolated and sulfonated as described below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06733947B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-789ad516cc7a459dbf3e7dacc4f95292 |
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| Source note | uspto-grants-2004_05 |
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