HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382252Generated: October 30, 2026
Oxalyl chloride → HCID 15281591, compound
https://huagongshe.com/reaction/382252
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-(4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)phenyl)acetic acid | HCID 16780847 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15281591 | HCID 15281591 | 59% |
Reaction Steps
1.0 g (4.33 mmol) of p-maleinimidophenylacetic acid were suspended in 25 ml of dichloromethane and diluted with a 2.5-fold excess of oxalic acid dichloride (1.37 g, 945 μl; 10.82 mmol). The reaction mixture was heated to 30-40° C. with the exclusion of moisture and stirred for 15 h. Then the solvent was removed under a vacuum and dried under a high vacuum. Crystallization from toluene yielded a yellow powder (yield: 59%); melting point: 154° C.; Rf-value: 0.29 (acetic ester/hexane 4/1); Elementary analysis: calculated: C: 58.91% H: 3.30% N: 5.75%, Cl: 14.49%; (C12H8NO3Cl) found: C: 60.61% H: 3.64% N: 5.13% Cl: 13.80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310039B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-e38485fd48354379bdd1a59678b550d3 |
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| Source note | uspto-grants-2001_10 |
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