HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352883Generated: October 29, 2026
Ethylene Glycol → HCID 22710203, compound
https://huagongshe.com/reaction/352883
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 22709577 | HCID 22709577 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22710203 | HCID 22710203 | — |
Reaction Steps
In toluene (10 mL) were dissolved 4-[(5-chloro-1-phenylsulfonylindol-2-yl)sulfonyl]-1-(tert-butoxycarbonyl)-2-(formylmethyl)piperazine (440 mg) and ethylene glycol (71 mg, followed by the addition of p-TsOH.H2O (15 mg). The resulting mixture was heated to 60° C. and stirred for 16 hours. Ethyl acetate was added to the reaction mixture. The resulting mixture was washed with a saturated aqueous solution of sodium bicarbonate. The organic layer was dried over anhydrous MgSO4 and distilled under reduced pressure to remove the solvent, whereby the title compound (460 mg) was obtained as colorless amorphous.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06747023B1 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-c6c5e0b01ac64504af4c8ef5d773d6d0 |
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| Source note | uspto-grants-2004_06 |
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