Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester | HCID 70670 | — |
| Reactant | Isopropyl Isothiocyanate | HCID 75263 | — |
| Reactant | Methyl 3-bromo-2-oxobutanoate | HCID 11183175 | — |
| Product | Isohexane ethyl acetate | HCID 21882781 | — |
| Product | HCID 69196361 | HCID 69196361 | — |
Reaction Steps
Ethoxycarbonylmethylene triphenyl phosphorane (33.8 g) in dry THF (200 ml) was treated with isopropyl isothiocyanate (10.1 g) at 65° C. for 16 h under nitrogen. The mixture was cooled to −78° C. and methyl 3-bromo-2-oxo-butanoate (19.5 g) was added. The reaction was allowed to warm slowly to room temperature. After 24 h at room temperature more methyl 3-bromo-2-oxo-butanoate (2.8 g) was added and the mixture was warmed to 60° C. for 16 h. The cooled reaction was poured into water (1.5 L) and extracted into ether. Drying and evaporation gave an oil which was chromatographed (SiO2/10:1 isohexane-ethyl acetate then 5:1 isohexane-ethyl acetate) to afford the subtitle compound (23.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07361660B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-d915d49ef73b40cf80367b83fae5e037 |
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| Source note | uspto-grants-2008_04 |
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