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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190900Generated: October 31, 2026

Dimethyl malonate → HCID 67523648, compound

https://huagongshe.com/reaction/2190900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl malonateHCID 7943—
ReactantSodium hydrideHCID 24758—
Reactant2-Acetoxybenzoyl chlorideHCID 79668—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67523648HCID 67523648—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of O-acetylsalicyloyl chloride (Alfa Aesar, 1.0 g, 5.05 mmol) in THF (10 mL) at 0° C. was added sodium hydride (60% dispersed in mineral oil, 263 mg, 6.57 mmol). It was stirred at 0° C. for 15 min prior to the addition of a solution of dimethyl malonate (0.67 g, 5.05 mmol) in THF (5 mL) at 0° C. The resulting mixture was stirred at 0° C. for 5 min and then at rt for 2.5 h, and was concentrated. The residue was taken up in water (50 mL), acidified by 1 N HCl aqueous solution, and extracted with EtOAc (2×100 mL). Combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated to give the intermediate (2-(2-acetoxy-benzoyl)-malonic acid dimethyl ester) (1.45 g) as an oil. The intermediate (1.26 g, 4.28 mmoL) was treated with (1/1) MeOH/10% aq HCl (26 mL) and heated to 75° C. (oil bath temperature) for 30 min and then at rt overnight. White precipitate formed during the reaction was collected, rinsed with water and dried in vacuo to give the title compound (555 mg). MS ESI(+) m/e: 221 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324405B2
Source datasetuspto-grants-2012_12
ORD IDord-bb4fed49587e48afb2026de797e3f77a
Source noteuspto-grants-2012_12