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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614658Generated: November 1, 2026

1-Hexanol → HCID 9864892, compound

https://huagongshe.com/reaction/1614658

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HexanolHCID 8103—
ReactantTriethylamineHCID 8471—
ReactantHCID 10615554HCID 10615554—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9864892HCID 986489225.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05198466
Source datasetuspto-grants-1993_03
ORD IDord-904e982296e642768da51d3277669e66
Source noteuspto-grants-1993_03