Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cyanide | HCID 5975 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1,2-Bis(bromomethyl)-4-methoxybenzene | HCID 10541786 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-Methoxy-o-phenylenediacetonitrile | HCID 70592541 | — |
Reaction Steps
Finely ground sodium cyanide (73 gm., 1.48 m) was suspended in dimethylsulfoxide (500 ml.) by means of a "Vibro-Mixer". A solution of 4-Methoxy-α,α'-dibromo-o-xylene (113 gm., 0.384 m) in dimethylsulfoxide (200 ml.) was added dropwise to the cyanide suspension. The internal temperature was kept at 35°-38° C. by means of an ice bath. The addition took 15 minutes. Agitation of the reaction was continued for a further 11/2 hours. The reaction mixture was poured into water (4 l.). The aqueous mixture was extracted with ether (2×1 l., 3×500 ml.) and the combined ether extracts were washed with dilute hydrochloric acid (6 N) (2×500 ml.), saturated sodium carbonate solution (1×500 ml.), water (3×500 ml.) and saturated sodium chloride solution (2×500 ml.). The ether layer was dried over magnesium sulfate. The dried ethereal solution was evaporated to an oil which was distilled and the fraction with boiling range 160°- 165° (0.1 mm) was collected. wt.=53 gm. The oil obtained was crystallized from ether (650 ml.) to give 45 gm. (m.p. 51°-53°). A second crop of 5.8 gm.(m.p. 49°-51°) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04210749 |
|---|
| Source dataset | uspto-grants-1980_07 |
|---|
| ORD ID | ord-383d636ed1dc4e83bc6936e2fd9a1318 |
|---|
| Source note | uspto-grants-1980_07 |
|---|