HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-n-Butyl-5-(2,4,5-trimethoxybenzylidene) hydantoin → 3-n-Butyl-5-(2,4,5-trimethoxybenzyl) hydantoin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-n-Butyl-5-(2,4,5-trimethoxybenzylidene) hydantoin | HCID 53964282 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-n-Butyl-5-(2,4,5-trimethoxybenzyl) hydantoin | HCID 12790722 | — |
Reaction Steps
3-n-Butyl-5-(2,4,5-trimethoxybenzylidene) hydantoin (10.0 g; 0.03 mole) was mixed with glacial acetic acid (150 ml.) and hydrogenated in a Parr apparatus in the presence of 5% Pd/C (2 g). After 2 hours the catalyst was filtered off, washed with warm acetic acid and the colourless filtrate evaporated in vacuo to give a white crystalline solid. Recrystallisation from ethyl acetate gave the title compound, yield 9.2 g (91% ), m.p. 122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04293563 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-ce3a288b229b4defa7c5dbe1380b8974 |
| Source note | uspto-grants-1981_10 |