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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443989Generated: October 31, 2026

Tetrabutylammonium Hydroxide → Isohexane ethyl acetate

https://huagongshe.com/reaction/1443989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium HydroxideHCID 2723671—
ReactantHCID 11180148HCID 11180148—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
ProductIsohexane ethyl acetateHCID 21882781—
ProductHCID 178494254HCID 178494254—

Reaction Steps

tetrabutylammonium hydroxide (0.28 g of 40% aqueous solution) was added to a solution of 2,3-dichloro-N-(5,6-dichloro-3-methoxy-2-pyrazinyl)-N-{[2-(trimethylsilyl)ethoxy]methyl}benzenesulfonamide (0.25 g) in 1,2-dimethoxyethane (3.0 mL) at room temperature. After 16 h, the solution was diluted with ethyl acetate (20 mL). The organic solution was washed with aqueous citric acid (10 mL) and brine, dried (MgSO4) and evaporated. Chromatography on silica gel eluting with ethyl acetate/isohexane mixtures gave the title compound containing the SEM group, as a white solid (0.08 g). The solid was dissolved in trifluroacetic acid (2.0 mL) and dichloromethane (2.0 mL) and stirred at room temperature for 1 h. The reaction mixture was concentrated and chromatography on silica gel eluting with ethyl acetate/isohexane mixtures gave the title compound as a white solid (0.027 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662825B2
Source datasetuspto-grants-2010_02
ORD IDord-2dc3ffcfe7e742dda562567b823bc21d
Source noteuspto-grants-2010_02