HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → ethyl 1-methyl-1H-benzofuro[2,3-g]indole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | ethyl 1H-benzofuro[2,3-g]indole-2-carboxylate | HCID 13438846 | — |
| Product | ethyl 1-methyl-1H-benzofuro[2,3-g]indole-2-carboxylate | HCID 15170283 | 86.3% |
Reaction Steps
Using the procedure outlined in Example 34A, ethyl 1H-benzofuro[2,3-g]indole-2-carboxylate (H. G. Pars Pharmaceutical Laboratories, Inc.) gave a 86.3% yield of ethyl 1-methyl-1H-benzofuro[2,3-g]indole-2-carboxylate, mp 114°-116°, (EtOAc), (C,H,N).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04999369 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-bbe1ef3df1f54ee096802a4e9cfefb57 |
| Source note | uspto-grants-1991_03 |