HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36765Generated: October 28, 2026
Toluene → N-(2,6-Diisopropylphenyl)-2-[2-(4-phenylpiperazinyl)ethylsulfonyl]acetamide
https://huagongshe.com/reaction/36765
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | N-(2,6-diisopropylphenyl)-2(2-chloroethylsulfonyl)acetamide | HCID 19937765 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(2,6-Diisopropylphenyl)-2-[2-(4-phenylpiperazinyl)ethylsulfonyl]acetamide | HCID 19937768 | 70.7% |
Reaction Steps
A mixture of 3.46 g of N-(2,6-diisopropylphenyl)-2(2-chloroethylsulfonyl)acetamide synthesized in (1) above, 1.62 g of N-phenylpiperazine, and 50 ml of toluene was heated under reflux for 4 hours. To the reaction mixture was added 100 ml of ethyl acetate, and the mixture was washed successively with a sodium hydrogencarbonate aqueous solution and a saturated sodium chloride aqueous solution, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was subjected to column chromatography using a mixture of ethyl acetate and hexane at a ratio varying from 1:1 to 1:0 as a developing solvent. The solvent was evaporated, and the residue was dissolved in ethyl acetate and crystallized from a 4N hydrochloric acid solution in ethyl acetate to obtain 3.33 g of the title compound as white powder (m.p.=197.0°-200.0° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05416212 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-2c01800daad5483f8931d0b7feb74107 |
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| Source note | uspto-grants-1995_05 |
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