HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403168Generated: October 29, 2026
Dichloromethane → HCID 10411615, compound
https://huagongshe.com/reaction/403168
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Tris(hydroxymethyl)aminomethane | HCID 6503 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | HCID 59016620 | HCID 59016620 | — |
| Product | HCID 10411615 | HCID 10411615 | — |
Reaction Steps
In a 25 mL vial, 123.1 mg (0.388 mmol) of 4-ethyl-benzoic acid N′-(1-tert-butyl-heptyl)-hydrazide were dissolved in 5 mL CH2Cl2. 3 equivalents of PS-NMM (polystyrene-SO2NH(CH2)3-morpholine, Argonaut Tech.) were added, followed by 3 mL CH2Cl2 to create a stirable suspension. One equivalent of acid chloride was added, and the reaction mixture was stirred overnight. The next day, 2 equivalents of AP-NCO resin (isocyante scavenger, ArgonautTech.) and 2 equivalents of AP-trisamine (polystyrene-CH2NHCH2CH2NH(CH2CH2NH2)2, Argonaut Tech.) were added with 3 mL CH2Cl2. The mixture was stirred for four hours and the resins were filtered. The reaction was analyzed by TLC, the solvent was removed, and the residue was dried under vacuum. After silica gel column chromatography using a 0-100% ether in hexane gradient, 107.5 mg of 2-methoxy-nicotinic acid N-(1-tert-butyl-heptyl)-N′-(4-ethyl-benzoyl)-hydrazide were isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748125B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-b9f6dbbd0f3e41509197df60b0e115be |
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| Source note | uspto-grants-2014_06 |
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