Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium diisopropylamide mono(tetrahydrofuran) | HCID 10997623 | — |
| Reactant | HCID 18960412 | HCID 18960412 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 18960407 | HCID 18960407 | 90% |
Reaction Steps
A solution of 25.2 g (0.10 mol) of N-(1,1-dimethylethyl)-2-isocyanobenzenemethanesulfonamide in 600 mL anhydrous THF was cooled to -70° C. under nitrogen atmosphere and treated with 147 mL (0.22 mol) 1.5M lithium diisopropylamide mono(tetrahydrofuran) in cyclohexane at such a rate as to keep the temperature under -60° C. The mixture was stirred at -70° C. for 15 minutes then warmed to 0° C. Saturated ammonium chloride solution (75 mL) was then added and the product was extracted with two 200 mL portions of ethyl acetate. The organic extract was washed with 10% HCl, brine, dried (MgSO4) and evaporated in vacuo. The resulting residue was triturated with ether/n-butyl chloride and collected by filtration to afford 22.7 g of the title compound, m.p. 157°-158° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05356862 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-2ac12c1408e44856888b5c8eb26a5730 |
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| Source note | uspto-grants-1994_10 |
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