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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415760Generated: October 26, 2026

Methyl acetoacetate → Methyl 2-(4-methylthiophenacyl)acetoacetate

https://huagongshe.com/reaction/1415760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl acetoacetateHCID 7757—
Reactant2-Bromo-4'-methylthioacetophenoneHCID 18368152—
ReactantPotassium tert-butoxideHCID 23665647—
SolventBenzeneHCID 241—
Solventtert-ButanolHCID 6386—
ProductMethyl 2-(4-methylthiophenacyl)acetoacetateHCID 5414342084.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05908858
Source datasetuspto-grants-1999_06
ORD IDord-8c6e5bc3c8044c15a75ac970763baaf7
Source noteuspto-grants-1999_06