HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 13686308, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 793248 | HCID 793248 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 13686308 | HCID 13686308 | — |
Reaction Steps
To a solution of 49.5 g of N-t-butyl-2-chlorobenzenesulfonamide in 875 mls of dry THF was added 262 ml of a 1.6M hexane solution of n-butyl lithium at -20° to -5° C. under an inert atmosphere. The mixture wasstirred at 0° C. for 1 hour, room temperature for 2 hours, recooled to -78° C. and contacted with 38 mls of dry dimethylformamide. The mixture was allowed to warm to room temperature overnight, poured into water, acidified to a ph of ~3 and ether extracted. The extract was washed with water and brine, dried over MgSO4 and concentrated to give a yellow oil. The oil was dissolved in 50% ether in hexane solution and allowed to stand, giving, after filtration, 38 g of the title compoundas colorless crystals, m.p. 139-141° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04867781 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-6c888596928947aca00ed0770876df1a |
| Source note | uspto-grants-1989_09 |