HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Hexanol → HCID 9864892, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Hexanol | HCID 8103 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 10615554 | HCID 10615554 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 9864892 | HCID 9864892 | 25.8% |
Reaction Steps
A solution of [[[2,6-bis(1 methylethyl)phenyl]amino]carbonyl]sulfamoyl chloride (5.0 g, 15.7 mmoles) in 80 mL THF was added dropwise to a solution of n-hexanol (1.60 g, 15.7 mmoles) and excess triethylamine (~3 mL) in 150 mL THF at room temperature under an atmosphere of N2. This was stirred for 16 hours and then concentrated in vacuo. The residue was partitioned between IN HCl and EtOAc and the organic layer was dried with MgSO4, filtered, and evaporated to give an oily tan solid. Trituration with acetone/hexanes (9:1) gave 1.56 g of the title compound as a white solid, mp 148-151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05198466 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-904e982296e642768da51d3277669e66 |
| Source note | uspto-grants-1993_03 |