HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → N-Isopropyl-2,3-xylidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 2,3-Dimethylaniline | HCID 6893 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-Isopropyl-2,3-xylidine | HCID 6454512 | — |
Reaction Steps
A mixture of 12 g of 2,3-xylidine, 60 ml of acetone and 30 g of type 5A sieves (alumino silicate) are placed in a flask and stirred overnight at room temperature. The mixture is filtered and the filtrate concentrated in vacuo to yield an oily residue. This residue is taken up in 100 ml of methanol, treated with 4.0 g of sodium borohydride and warmed to above 15° C. The mixture is made acidic, then basic, and finally extracted with ether to yield 11.4 g of N-isopropyl-2,3-xylidine which is verified by infra-red spectra and NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04021483 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-ee2e2749ac4746828c04221a19987cfd |
| Source note | uspto-grants-1977_05 |