HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrapropoxymethane → 3-Cyano-2-(1,1-dipropoxymethylenamino) thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrapropoxymethane | HCID 548455 | — |
| Reactant | 2-Aminothiophene-3-carbonitrile | HCID 736607 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | 3-Cyano-2-(1,1-dipropoxymethylenamino) thiophene | HCID 22995827 | — |
Reaction Steps
In a small distillation apparatus a mixture of 12.4 g(0.1 mol) 2-amino-3-cyanothiophene and 37.2 g (0.15 mol) tetra-n-propylorthocarbonate is heated for 3 hours at 155° C. n-PrOH, which arises during the reaction is directly distilled out of the reaction flask. After completion of the reaction, excess tetra-n-propylorthocarbonate is distilled off under reduced pressure and the resulting raw material purified by column chromatography over silica gel (eluant: hexane/tert.butylmethyl ether 6:1). Yield: 10.6 g of 3-cyano-2-(1,1-dipropoxymethyleneamino)thiophene in the form of slightly brownish crystals; m.p. 65-67° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06617330B2 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-11989f58923544e1b97262d0622e4d2e |
| Source note | uspto-grants-2003_09 |