Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (4-Iodobutyl)benzene | HCID 12709818 | — |
| Reactant | HCID 19605253 | HCID 19605253 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19605261 | HCID 19605261 | 14% |
Reaction Steps
A solution 4-(benzylthio)azetidin-2-one (1.1 g, 5.5 mmol) in dry THF (10 ml) was added dropwise over 10 minutes to a suspension of NaH (0.13 g, 5.6 mmol) in dry THF (5 ml) at -20° C. under a N2 atmosphere. A solution of 1-iodo-4-phenylbutane (1.4 g, 5.5 mmol) in dry THF (10 ml) was added dropwise over 10 minutes at -55° C. After stirring for 18 hours, the mixture was poured onto ice/water (50 g), filtered through hyflo, the THF evaporated under reduced pressure and the residue taken up in ethyl acetate. The solution was washed with brine (×2), dried (MgSO4), evaporated under reduced pressure to a yellow oil which was purified by flash chromatography on silica gel eluted with 5:1, 3:1 then 1:1 petroleun ether/ethyl acetate to give the product as a yellow oil (0.25 g, 14%). 1H NMR δ (CDCl3) 1.5 (4H, m, 2×CH2), 2.6 (2H, m, CH2Ph), 2.85, 3.2 (each 2H, m, H-3 & NCH2), 3.73 (2H, s, SCH2), 4.54 (1H, m, H-4), 7.2 (10H, m, 2×Ph--H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05990102 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-0d821eb87dee43209886bb2860a69f69 |
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| Source note | uspto-grants-1999_11 |
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