HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 838913Generated: October 25, 2026
Acrylonitrile → 3-((4-(2,2-Dichloro-1,1-difluoroethoxy)-2-methyl-5-nitrophenyl)sulfonyl)-2-propenenitrile
https://huagongshe.com/reaction/838913
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | 4-(2,2-Dichloro-1,1-difluoroethoxy)-2-methyl-5-nitrobenzenesulfonyl chloride | HCID 20325261 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-((4-(2,2-Dichloro-1,1-difluoroethoxy)-2-methyl-5-nitrophenyl)sulfonyl)-2-propenenitrile | HCID 54330210 | 10.4% |
Reaction Steps
In a 100 ml Fisher-Porter pressure vessel were placed 9.0 g (0.024 mol) of 4-(2,2-dichloro-1,1-difluoroethoxy)-2-methyl-5-nitrobenzenesulfonyl chloride, 2.4 g (0.048 mol) acrylonitrile, 2 ml acetonitrile, 0.07 g cupric chloride and 0.12 g triethylamine hydrochloride. After cooling and evacuating the vessel to 5 mm mercury pressure, it was sealed and heated in an oil bath at 105°-110° C for 38 hours. The vessel was opened and the reaction medium was filtered with the aid of benzene. The insolubles were discarded and the filtrate was treated with 5.0 g of triethylamine, refiltered, and washed with water. After decolorizing wth charcoal and drying over MgSO4, removal of the solvent under reduced pressure afforded a dark amber oil. Recrystallization from methanol provided 1.0 g of the title compound as a white solid, m.p. 109° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04093644 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-a5721f3dde8547abb817f25126565cce |
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| Source note | uspto-grants-1978_06 |
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