HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Benzene, 1-(2-chloroethyl)-2-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Nitrophenethyl alcohol | HCID 27054 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Benzene, 1-(2-chloroethyl)-2-nitro- | HCID 11030510 | 87% |
Reaction Steps
2.1 ml abs. pyridine and 21.62 g thionyl chloride (13.3 ml,. 0.18 mol) is added to 10.13 9 2-(2-nitrophenyl)ethanol (60 mmol) in 36 ml abs. toluene. After 2 h reflux, this is cooled and poured onto ice. The ice water is mixed with 50 ml chloroform and extracted 2× each with 50 ml chloroform. The combined organic phases are neutralized 2× each with 100 ml saturated bicarbonate solution. After drying with Na2SO4, this is filtered and rotary evaporated. After distillation under high-vacuum, 9.7 9 (50 mmol,. 87%) 2-(2-nitrophenyl)ethyl chloride is obtained as a yellow oil with a boiling point of 66 to 67° C. (0.001 mbar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06153744 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-3762e9a8787142ef847b3c5c10053b91 |
| Source note | uspto-grants-2000_11 |