Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451294Generated: November 2, 2026

Dimethyl acetylenedicarboxylate → HCID 178418309, compound

https://huagongshe.com/reaction/1451294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl acetylenedicarboxylateHCID 12980—
ReactantMethyl 2-amino-6-chlorobenzoateHCID 592849—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
ProductHCID 178418309HCID 17841830980.4%

Reaction Steps

A solution of methyl 2-amino-6-chlorobenzoate (3.00 g, 16.2 mM) and dimethyl acetylenedicarboxylate (2.64 g, 18.6 mM) in t-butanol (25 mL) was refluxed under a nitrogen atmosphere for 18 hr. The reaction mixture was cooled to room temperature and potassium t-butoxide (2.09 g, 18.6 mM) was added in one portion whereupon a precipitate formed. After refluxing this mixture for 1.5 hr, it was cooled to room temperature and filtered to separate the solids. The solids were dissolved in water and the resulting solution acidified with 1N H2SO4 to form a precipitate. The mixture was filtered and the collected solids were washed with water and air dried to give dimethyl 5-chloro-4-hydroxyquinoline-2,3-dicarboxylate (3.84 g, 80.2%) as a tan solid. An 0.25 g portion of this material was recrystallized from ethyl acetate to provide an analytical sample (0.152 g) of the title compound as an off-white solid, mp 174°-176° C.; MS(CI): 296 (M+H). Analysis for C13H10ClNO5 ·0.01H2O: Calculated: C, 52.78; H, 3.41; N, 4.73 Found: C, 52.39; H, 3.38; N, 4.67

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604227
Source datasetuspto-grants-1997_02
ORD IDord-1be74e35e8cc413d8b35af04cf2f7dbc
Source noteuspto-grants-1997_02