HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichlorobenzyl chloride → N,N-Dibutyl-N-[(2,4-dichlorophenyl)methyl]butan-1-aminium chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichlorobenzyl chloride | HCID 7212 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N,N-Dibutyl-N-[(2,4-dichlorophenyl)methyl]butan-1-aminium chloride | HCID 165101 | — |
Reaction Steps
Eighteen and fifty-four one-hundredths parts of tributylamine and 19.54 parts of 2,4-dichlorobenzyl chloride were placed in a 250 ml. glass stoppered flask. 70.8 parts of diethyl ether was added and the flask tightly stoppered and allowed to react at room temperature. After a considerable time an oil began to form and after 2 to 3 months, the product began to crystallize. At the end of six months, the crystals were filtered, washed with hexane and dried under vacuum. 16.7 parts of tributyl-2,4-dichlorobenzylammonium chloride was obtained, the compound having 3.33% nitrogen, the calculated value for nitrogen (for C19H32Cl3N) is 3.69%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04299618 |
| Source dataset | uspto-grants-1981_11 |
| ORD ID | ord-0e323a29d35e450894cee8251a780659 |
| Source note | uspto-grants-1981_11 |