HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635859Generated: November 1, 2026
m-Chloroperbenzoic acid → HCID 85040066, compound
https://huagongshe.com/reaction/1635859
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-Chloro-4-(3-dimethylaminopropyn-1-yl)-benzoic acid methyl ester | HCID 53979284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 85040066 | HCID 85040066 | — |
Reaction Steps
Gradually, 3-chloroperoxybenzoic acid (10.76 g) was added to a solution of 2-chloro-4-(3-dimethylamino-propyn-1yl)-benzoic acid, methyl ester (15.07 g in dichloromethane (40 ml), at a rate to maintain the reaction temperature at −20° C. The mixture was stirred for 10-15 minutes. The resulting N-oxide was purified by chromatography on Activity Grade I basic alumina (215 g), eluting with 10% methanol/dichloromethane. The solvent was evaporated in vacuo between 12 to 18° C. The resulting residue was dissolved in methanol (100 ml) and heated at 60-65° C. with stirring for 18 hours. After removing the solvent in vacuo, and the product was purified by column chromatography on silica gel (190 g), eluting with 70% ethyl acetate/hexane. Trituration with diethyl ether containing some hexane afforded the title compound as a solid (5.68 g), m.p. 92-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06511974B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-7b562549922444498e09ca1cfeba8d2d |
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| Source note | uspto-grants-2003_01 |
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