HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Acetyloxy)acetonitrile → (Acetyloxy)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Acetyloxy)acetonitrile | HCID 13843 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 15767077 | HCID 15767077 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (Acetyloxy)acetonitrile | HCID 13843 | — |
| Product | HCID 15767078 | HCID 15767078 | — |
Reaction Steps
Cyanomethyl acetate was prepared according to the method described in Synth. Commun. 2, 215 (1972). A mixture of 2.78 g (10 millimole) of tetrabutylammonium chloride and 1 g (10 millimole) of cyanomethyl acetate was dissolved in 10 ml of dichloromethane. To the reaction mixture were added 2 g (9.6 millimoles) of N-formyl-2,6 dichloro-4-fluoroaniline and 3 ml (12 millimoles) of a 4 mole/l sodium hydroxyde aqueous solution. After stirring for 1 hour at room temperature, N-cyanomethyl-N-formyl-2,6-dichloro-4-fluoroaniline was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05393913 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-37806c01b6be454aa580efc0e855b3bd |
| Source note | uspto-grants-1995_02 |