HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 4372276, compound → HCID 131710394, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 4372276 | HCID 4372276 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | HCID 131710394 | HCID 131710394 | — |
Reaction Steps
of ethyl(2-methyl-5-nitro-1,3-benzodioxol-2-yl)-acetate (prepared according to G. Sloof, Rec. Trav. Chim. 547, 995 (1935)) dissolved in 300 cc. of 95% alcohol are hydrogenated at room temperature and 2 atm. of hydrogen pressure in the presence of 6 g. of Raney nickel. After the theoretical absorption of hydrogen, the mixture is filtered and evaporated to dryness. The residual oil is purified by distillation, (b.p. 190°-200°C./0.4 mm.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03969368 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-7af12781928f4fb896fb6b08c56a6d00 |
| Source note | uspto-grants-1976_07 |