HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → [1,1':3', 1"-Terphenyl]-2'-yl[[[2,6-bis(1-methylethyl)phenyl]amino]sulfonyl]carbamat
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diisopropylaniline | HCID 32484 | — |
| Reactant | [1,1':3',1"-Terphenyl]-2'-yl(chlorosulfonyl)carbamate | HCID 10572313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [1,1':3', 1"-Terphenyl]-2'-yl[[[2,6-bis(1-methylethyl)phenyl]amino]sulfonyl]carbamat | HCID 10506346 | — |
Reaction Steps
A solution of [1,1':3', 1"-terphenyl]-2'-yl(chlorosulfonyl)carbamate (5.0 g, 12.9 mmol) in 75 mL tetrahydrofuran was added dropwise to a solution of 2,6-diisopropyl aniline (2.29 g, 12.9 mmol) and triethylamine (1.3 g, 12.9 mmol) in 100 mL tetrahydrofuran at -15° C. under an atmosphere of nitrogen. The resulting mixture was warmed to room temperature and stirred for 16 hours. Concentrated in vacuo and partitioned the residue between water and ethyl acetate. Dried the organic layer over MgSO4 and evaporated to give an off-white solid. Chromatography on silica gel gave the title compound, mp 166°-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05336690 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-f09b8a53804a4aa4abd7076939c4f1b7 |
| Source note | uspto-grants-1994_08 |