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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 498242Generated: October 26, 2026

Sulfuric Acid → 3-[3-(2-Methyl-pyrimidin-4-yl)-phenyl]-3-oxo-propionic acid tert-butyl ester

https://huagongshe.com/reaction/498242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant3-Acetylbenzoic acidHCID 220324—
ReactantN-(Bis-acetylamino-methyl)-acetamideHCID 536854—
ReactantMethyl 3-(2-methylpyrimidin-4-yl)benzoateHCID 17174862—
SolventWaterHCID 962—
Product3-[3-(2-Methyl-pyrimidin-4-yl)-phenyl]-3-oxo-propionic acid tert-butyl esterHCID 69486722—

Reaction Conditions

Temperature155 °C

Reaction Steps

The title compound was prepared from 3-(2-methyl-pyrimidin-4-yl)-benzoic acid methyl ester [prepared by the following procedure: A mixture of 3-acetyl-benzoic acid (0.82 g, 5 mmol), N-(bis-acetylamino-methyl)-acetamide (0.94 g, 5 mmol) and conc. H2SO4 (0.01 ml) was heated to 155° C. for 6 h. The cooled mixture was diluted with H2O (20 ml) and the precipitate was collected, dried and esterified by heating in MeOH (12 ml)/4N HCl-Et2O (3 ml) for 20 h at 40° C.; white crystals (0.27 g).] (0.80 g, 3.5 mmol by treatment with lithium tert-butyl acetate according to general procedure K (method b). Obtained as a yellow solid (1.36 g, crude product).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949542B2
Source datasetuspto-grants-2005_09
ORD IDord-9acf5ee7dc8247b589bee8b4fb99d2a0
Source noteuspto-grants-2005_09