HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846974Generated: November 2, 2026
Methyl Methacrylate → HCID 86731823, compound
https://huagongshe.com/reaction/1846974
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Methacrylate | HCID 6658 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 86731822 | HCID 86731822 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86731823 | HCID 86731823 | — |
Reaction Steps
Methyl methacrylate (125.0 g, 1097 mmol) and potassium tert-butoxide (1 M in tetrahydrofuran, 115 mL, 115 mmol) were sequentially added to a solution of 1-(4-chloro-3-fluorophenyl)-2-(3-chlorophenyl)ethanone (327.0 g, 1160 mmol, Example 4, Step B) in anhydrous tetrahydrofuran (2.61 L), at 0° C. The reaction mixture was stirred for 1 hour at 0° C. and then warmed to ambient temperature and stirred for 12 hours. On completion, the reaction was quenched with water (1.0 L) and extracted with ethyl acetate (2×2.5 L). The combined organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to get the crude material which was purified by flash column chromatography (silica gel: 60 to 120 mesh, product eluted in 4% ethyl acetate in hexane) affording the title compound (mixture of diastereomers) as light yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952036B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-4c754db4bdc34781b8743eea508519b8 |
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| Source note | uspto-grants-2015_02 |
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