HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898839Generated: October 29, 2026
Diethyl Malonate → Diethyl 2-[1-(4-fluorophenyl)-1-methyl-2-methylsulfanyl-ethyl]malonate
https://huagongshe.com/reaction/898839
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Ethanol sodium ethoxide | HCID 23706232 | — |
| Reactant | 1-(2-Chloro-1-methyl-1-methylsulfanyl-ethyl)-4-fluorobenzene | HCID 59692380 | — |
| Reactant | 1-(1-Chloro-1-methyl-2-methylsulfanyl-ethyl)-4-fluorobenzene | HCID 59692580 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl 2-[1-(4-fluorophenyl)-1-methyl-2-methylsulfanyl-ethyl]malonate | HCID 59692402 | 84% |
Reaction Steps
To a solution of diethyl malonate (12 mL, 81 mmol) in ethanol (40 mL) was added dropwise 21% sodium ethoxide ethanol solution (29 mL, 77 mmol) under nitrogen atmosphere under ice-cooling. The mixture was warmed to room temperature, stirred for 1 hour, and cooled again with ice. The crude product (73 mmol) of 1-(1-chloro-1-methyl-2-methylsulfanyl-ethyl)-4-fluorobenzene or 1-(2-chloro-1-methyl-1-methylsulfanyl-ethyl)-4-fluorobenzene obtained in Example 1-3 was added dropwise to the mixture while maintaining a temperature below 4° C. The obtained solution was stirred for 1 hour at room temperature and concentrated under reduced pressure. The residue was neutralized by adding a 2N aqueous hydrochloric acid solution and the aqueous layer was extracted with ethyl acetate (50 mL). The organic layer was dried over magnesium sulfate, filtrated and the solvent was evaporated. Then the obtained residue was purified by silica gel chromatography (hexane:ethyl acetate=20:1 to 5:1) to give the title compound (24 g, yield 84%) as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07351825B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-f79963e9fb9d489c87652dae8595c891 |
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| Source note | uspto-grants-2008_04 |
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