HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856829Generated: October 26, 2026
Methyl acetoacetate → Methyl 2-(4-methylthiophenacyl)acetoacetate
https://huagongshe.com/reaction/856829
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | 2-Bromo-4'-methylthioacetophenone | HCID 18368152 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | Methyl 2-(4-methylthiophenacyl)acetoacetate | HCID 54143420 | 84.9% |
Reaction Steps
2.28 g (19.7 mmol) of methyl acetoacetate were dissolved in 40 ml of 2-methyl-2-propanol, and 2.21 g (19.7 mmol) of potassium t-butoxide were added to the resulting solution under a nitrogen atmosphere. The mixture was then stirred at room temperature for 1 hour, after which a solution of 4.82 g (19.7 mmol) of 4-methylthiophenacyl bromide in 30 ml of benzene was added dropwise to the resulting mixture. The mixture was then stirred at 60° C. for 3 hours, after which it was cooled. It was then poured into ice-water and extracted with ethyl acetate. The organic extract was washed with a saturated aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure. The resulting residue was applied to a silica gel chromatography column and eluted with a 1:4 by volume mixture of ethyl acetate and hexane, to give 4.42 g (yield 80%) of the title compound as a slightly yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE039420E1 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-241a11310d504dc5b9d0bc90faac8d79 |
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| Source note | uspto-grants-2006_12 |
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