Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 13577545 | HCID 13577545 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13577548 | HCID 13577548 | — |
Reaction Steps
3-(5,6-Dihydro-1,4,2-oxathiazine-3-yl)benzoic acid (15 g, 0.07 mol) was suspended in methylene chloride (200 ml). Thionyl chloride (10 ml) was added and the reaction was refluxed until homogeneous and all gassing had ceased. The solvent was removed, the remaining oil was taken up in methylene chloride and treated portionwise with aniline (12.5 g, 0.12 mol). An exotherm was observed. After several hours, water was added, the organic material separated, washed successively with water, aqueous bicarbonate, dilute hydrochloric acid, water and then dried over anhydrous magnesium sulphate. Evaporation of the solvent left a solid which was recrystallised from ethanol to give crystals of 3-(5,6-dihydro-1,4,2-oxathiazin-3-yl)-N-phenylbenzamide, mp 149°-150° C. (Found: C, 64.65; H, 4.92; N, 9.65. C16H14N2O2S requires C, 64.42; H, 4.73; N, 9.39).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04675044 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-39bf086bc9f34e9780a20347d313b5d4 |
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| Source note | uspto-grants-1987_06 |
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