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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968942Generated: October 30, 2026

Dichloromethane → HCID 10411615, compound

https://huagongshe.com/reaction/968942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
Reactant4-MethylmorpholineHCID 7972—
ReactantHCID 59016620HCID 59016620—
ProductHCID 10411615HCID 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, Argonaut Tech.) 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304161B2
Source datasetuspto-grants-2007_12
ORD IDord-3a44a6a7b4564f0695cb818eff939ba1
Source noteuspto-grants-2007_12