Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | HCID 20220107 | HCID 20220107 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13784627 | HCID 13784627 | 33.1% |
Reaction Steps
To a solution of 6.26 g of 2-aminothiophenol in 50 ml of dimethylformamide was added 9.85 g of 2-bromo 5-hydroxyvaleric acid. The mixture was stirred at room temperature for 2 hours and at 100° C. for 1 hour. The reaction solution was cooled, poured into water, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4) and then concentrated under reduced pressure. The concentrate was subjected to a column chromatography on silica-gel (200 g). From the eluate with hexane-acetone (2:1, v/v) was obtained 3.7 g (31.6%) of 2-(3-hydroxypropyl)-2H-1,4-benzothiazin-3(4H)-one as crystals. Recrystallization from ethyl acetate-hexane gave prisms, m.p. 59°-60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04640916 |
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| Source dataset | uspto-grants-1987_02 |
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| ORD ID | ord-1a2bfec95d314090b9ab1dba7e6940ff |
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| Source note | uspto-grants-1987_02 |
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