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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495972Generated: October 30, 2026

Dimethyl acetylenedicarboxylate → HCID 178418477, compound

https://huagongshe.com/reaction/495972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl acetylenedicarboxylateHCID 12980—
ReactantMethyl 4-chloroanthranilateHCID 80001—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
ProductHCID 178418477HCID 17841847747%

Reaction Steps

A stirred mixture of methyl 2-amino-4-chlorobenzoate (2.50 g, 13.5 mmol) and dimethyl acetylenedicarboxylate (2.05 g, 14.4 mmol) in tert-butanol (22 ml) was refluxed for 7 hours under a nitrogen atmosphere. After adding additional dimethyl acetylenedicarboxylate (1.16 g, 8.13 mmol) and refluxing another 2.5 hours, the reaction mixture was allowed to cool to room temperature and potassium tert-butoxide (1.56 g, 13.9 mmol) was added in one portion. A precipitate formed and the resulting mixture was refluxed for 1.5 hours. The mixture was cooled to room temperature and filtered to separate the solids, which were washed with tert-butanol and ether. The solids were dissolved in water and acidified with 1 N sulfuric acid to form a precipitate. The resulting mixture was extracted with methylene chloride and the combined extracts were washed with brine and water, dried over MgSO4, filtered and concentrated to give a green solid. Recrystallization of this material from methanol provided the title compound (1.15 g, 47%) as an off-white solid, mp 232–233° C.; MS (CI):296 (M+H). Analysis for C13H10ClNO5: Calc'd: C, 52.81; H, 3.41; N, 4.74; Found: C, 52.75; H, 3.47; N, 4.69.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06943165B2
Source datasetuspto-grants-2005_09
ORD IDord-7190fe90047044d59f81743d23abe573
Source noteuspto-grants-2005_09