HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 67785432, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | HCID 19384475 | HCID 19384475 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67785432 | HCID 67785432 | — |
Reaction Steps
To a mixture of 3.7 g of the aldehyde derivative from Example 155, 2.0 g of sodium cyanide and 10 g of activated manganese dioxide in 200 mL of methanol was added 1.0 g of acetic acid at room temperature. The reaction mixture was stirred for 2 hours at room temperature, filtered on celite and extracted with ethyl acetate. The crude material (3.5 g) was purified on a short pad of silica gel giving 2.9 g (73%) of 5-[(1,2,3,4-tetrahydro-9-octyl-9H-dibenzo[b,d]pyrrol-6-yl)carbonyl]-2-furancarboxylic acid methyl ester as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05451600 |
| Source dataset | uspto-grants-1995_09 |
| ORD ID | ord-dfe94bb5e6794b14b5d11c61033a9212 |
| Source note | uspto-grants-1995_09 |