HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (3-Nitro-benzyl)dipropylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dipropylamine | HCID 8902 | — |
| Reactant | alpha-Chloro-m-nitrotoluene | HCID 12078 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | (3-Nitro-benzyl)dipropylamine | HCID 13022589 | — |
Reaction Steps
To a solution of 5.13 g of m-nitro-benzyl chloride in 100 ml benzene at 10° C. was added in small portions 6.2 g of dipropylamine over a period of 15 minutes. The reaction mixture was stirred and allowed to come to room temperature for 1.5 hours, and was then refluxed for 4 hours. Water was added to the solution and the organic layer was separated and collected. The organic layer was washed with water (3×100 ml), dried (MgSO4) and stripped to leave a dark-red oil. The product (Compound No. 1) was chromatographed over silica gel (hexane: CH2Cl2 ; 1.0:0; 4:1), to yield the title product as a yellow-amber oil. Analysis: C: calculated, 66.08; found, 65.38. H: calculated, 8.53; found 8.55. N: calculated, 11.85; found, 11.73.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04339461 |
| Source dataset | uspto-grants-1982_07 |
| ORD ID | ord-d800e62ba88e4adaad1b3b2fdb7f8f55 |
| Source note | uspto-grants-1982_07 |