HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207867Generated: November 2, 2026
Iodopentafluoroethane → 4,4,5,5,5-Pentafluoro-1-(3'-methylsulfanyl-biphenyl-4-yl)-pent-1-en-3-one
https://huagongshe.com/reaction/2207867
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodopentafluoroethane | HCID 9636 | — |
| Reactant | N-methoxy-N-methyl-3-(3'-methylsulfanyl-biphenyl-4-yl)-acrylamide | HCID 131735932 | — |
| Reactant | HCID 178419607 | HCID 178419607 | — |
| Product | 4,4,5,5,5-Pentafluoro-1-(3'-methylsulfanyl-biphenyl-4-yl)-pent-1-en-3-one | HCID 131735933 | 76.2% |
Reaction Steps
To a saturated solution of pentafluoroiodoethane (0.84 M, in diethyl ether) (203.5 mL, 162.8 mmol), was slowly added methyllithium/lithium bromide (1.5 M, in diethyl ether) (108.6 mL, 162.8 mmol) under nitrogen atmosphere at −78° C. The reaction mixture was stirred for 20 minutes and then a solution of N-methoxy-N-methyl-3-(3′-methylsulfanyl-biphenyl-4-yl)-acrylamide (17.0 g, 54.3 mmol, in tetrahydrofuran 20.0 mL) prepared in Step 1 was slowly added thereto at −78° C. The reaction mixture was stirred at room temperature, quenched with distilled water, acidified by a 10% potassium hydrogen sulfate solution (pH=5), and then extracted with diethyl ether three times. The combined extract was washed with a saturated solution of sodium hydrogen carbonate, dried on anhydrous magnesium sulfate, and then concentrated under reduced pressure to give a yellow liquid residue. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/30) to give 15.4 g of the titled compound as a yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376420B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-1064b2f6614d45f59c2f2b23c9fd7817 |
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| Source note | uspto-grants-2016_06 |
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