HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585473Generated: October 30, 2026
Dimethyl acetylenedicarboxylate → HCID 178418477, compound
https://huagongshe.com/reaction/585473
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl acetylenedicarboxylate | HCID 12980 | — |
| Reactant | Methyl 4-chloroanthranilate | HCID 80001 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 178418477 | HCID 178418477 | 47% |
Reaction Steps
A stirred mixture of methyl 2-amino-4-chlorobenzoate (2.50 g, 13.5 mmol) and dimethyl acetylene dicarboxylate (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 diethyl ether. The solids were dissolved in water and acidified with 1 N sulfuric acid to form a precipitate. The resulting mixture was extracted with DCM 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 (Cl): 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06933297B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-3fb57db538f1428a91c5f92cf3652db2 |
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| Source note | uspto-grants-2005_08 |
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