HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443989Generated: October 31, 2026
Tetrabutylammonium Hydroxide → Isohexane ethyl acetate
https://huagongshe.com/reaction/1443989
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| Reactant | HCID 11180148 | HCID 11180148 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Isohexane ethyl acetate | HCID 21882781 | — |
| Product | HCID 178494254 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662825B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-2dc3ffcfe7e742dda562567b823bc21d |
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| Source note | uspto-grants-2010_02 |
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