HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Chloro-2-(chloromethyl)-1-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Chloro-2-nitrobenzyl alcohol | HCID 556066 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Chloro-2-(chloromethyl)-1-nitrobenzene | HCID 12595970 | 99% |
Reaction Steps
To a solution of 5-chloro-2-nitrobenzyl alcohol (80 g, 0.42 mol) and triethylamine (64 ml, 0.46 mol) in dichloromethane (840 ml) was added drop wise thionyl chloride (34 ml, 0.46 mol) during a period of 30 minutes while the internal temperature was kept below 32° C. by cooling with a water bath. The reaction mixture was stirred for 3 h. The solvent was evaporated and the residue was triturated in warm tert-butyl methyl ether (970 ml). The ammonium salts were removed by filtration and the filtrate was concentrated in vacuo to give the title compound (85 g, 99%) as brown oil which was used in the next step without purification. MS m/e: 205 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492376B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-ab7aefc6ae044fbf99584cf0a899d209 |
| Source note | uspto-grants-2013_07 |