HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl isocyanate → Formamide, N-1-naphthalenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | alpha-Naphthyl isocyanate | HCID 66589 | — |
| Product | Formamide, N-1-naphthalenyl- | HCID 96004 | 94% |
Reaction Steps
The catalytic hydrogenation procedure of Example 1 was repeated except that the phenyl isocyanate used therein was replaced by 1.7 g. (0.01 mole) of 1-naphthylisocyanate. Reduction was complete in 45 minutes. The catalyst was removed by filtration and the colorless filtrate then evaporated to dryness giving 1.71 g. of tan-white crude product, m.p. 134° - 135° C. The solid was recrystallized from ethanol-water to give 1.62 g. (94% yield) of dried title product, m.p. 137.5° - 138.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04125724 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-8825c44c40eb4b4e97de72d748172e3a |
| Source note | uspto-grants-1978_11 |