Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 140352840 | HCID 140352840 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 88627039 | HCID 88627039 | 23% |
Reaction Steps
Ethyl (Z)-2-(tetrahydrothien-3-yloxyimino)-3-oxo-butyrate (1.29 g) was dissolved in a mixture of carbontetrachloride (15 ml), dichloromethane (5 ml) and methanol (2 ml). The mixture was cooled to -26°, a solution of hydrogen bromide in acetic acid (0.05 ml, 45% w/v) was added followed by bromine (0.29 ml). The mixture was allowed to warm to room temperature and stirred for 3 dyys. The solvents were removed under reduced pressure, the residue was partitioned between ethyl acetate and water. The organic layer was washed successively with saturated aqueous sodium bicarbonate, water and brine, then dried (MgSO4) and evaporated. Purification by flash chromatography with dichloromethane elution gave the title compound (0.4 g, 23%) as a pale yellow liquid. νmax (film) 2970, 2940, 1740, 1695, and 1600 cm-1. δH (CDCl3) 1.34 (3H, t), 2.04 (1H, m), 2.48 (1H, m), 2.90 (2H, m), 3.13 (2H, m), 4.33 (2H, s), 4.37 (2H, q), and 5.18 (1H, m). [Mass spectrum: +ve ion MH+ (324)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04816452 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-55ed3f60085f4200849bff1612831fc2 |
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| Source note | uspto-grants-1989_03 |
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