HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501243Generated: October 26, 2026
Hydrochloric Acid → Phenyl 3-methyl-3-nitrobutane-1-sulfonate
https://huagongshe.com/reaction/501243
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Nitropropane | HCID 398 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Phenyl ethenesulfonate | HCID 564920 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Phenyl 3-methyl-3-nitrobutane-1-sulfonate | HCID 86616499 | — |
Reaction Steps
A mixture of 9.43 g of phenyl ethenesulfonate and 4.60 ml of 2-nitro-propane was heated to 80° C. and, at 80° C., 0.89 ml of ethyidiisopropylamine was added dropwise. The mixture was stirred at 80° C. for 4 hours and 30 minutes, left to stand at RT for 16 hours and then stirred at 80° C. for a further 2 hours. Cooling to RT was followed by addition of 250 ml of a 2N aqueous HCl solution and extraction 3 times with 150 ml of EA each time. Drying over Na2SO4 and removal of the solvent in vacuo were followed by coevaporation 3 times with 100 ml of toluene each time. 13.47 g of a pale yellow oil were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772262B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-6087daf0a21747a5a9e520a04e85a4ec |
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| Source note | uspto-grants-2010_08 |
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