HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659957Generated: October 30, 2026
4-Fluorophenylacetyl chloride → HCID 68430510, compound
https://huagongshe.com/reaction/659957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorophenylacetyl chloride | HCID 3744988 | — |
| Reactant | 4-Iodo-2-(methylthio)pyrimidine | HCID 3858901 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68430510 | HCID 68430510 | 45.8% |
Reaction Steps
20 g (79 mmoles) of 4-iodo-2-methylthiopyrimidine in 165 mL of tetrahydrofuran under argon is cooled to −70° C. 45.5 mL of isopropylmagnesium chloride (2M in THF) is then slowly added to the reaction mixture, keeping the temperature at −70° C. After 30 min., a solution of 4-fluorophenyl acetyl chloride (13.7 g, 79 mmoles) in 65 mL tetrahydrofuran is added dropwise to the reaction mixture which is further stirred at −78° C. for 1 hour and allowed to reach 0° C. After 30 min. at 0° C., the reaction is poured into ice-water and extracted with ethyl acetate. The organic phase is washed with water and dried over magnesium sulfate. After concentration the oily purified by chromatography on silica gel (ethyl acetate/hexane 4/1) affording 9.5 g of 2-(4-Fluoro-phenyl)-1-(2-methylthio-pyrimidin-4-yl)-ethanone as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084395B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-b9ba12bb0c79476d9d6727c98de1d271 |
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| Source note | uspto-grants-2011_12 |
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