HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 1-(1-Isocyanopentane-1-sulfonyl)-4-methylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(1-Isocyanopentane-1-sulfonyl)-4-methylbenzene | HCID 45789946 | 86% |
Reaction Steps
A mixture of p-toluenesulfonylmethyl isocyanide (9.75 g), tetrabutylammonium iodide (3.69 g), 1-butyl iodide (11.3 mL), dichloromethane (100 mL) and 30% aqueous sodium hydroxide solution (100 mL) was stirred at room temperature for 12 hr. The reaction product was diluted with water (200 mL), and extracted with dichloromethane. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained gum-like residue was extracted 3 times with diethyl ether (100 mL). The extract was concentrated under reduced pressure to give the title compound as a colorless oil (yield 10.8 g, 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08048909B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-91cdd8401df645859ef2931e19cb2ae1 |
| Source note | uspto-grants-2011_11 |