HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl indole-2-carboxylate → Ethyl 3-(4-benzyloxybenzhydryl)indole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl indole-2-carboxylate | HCID 73125 | — |
| Reactant | 4-Benzyloxybenzhydrol | HCID 10589580 | — |
| Product | Ethyl 3-(4-benzyloxybenzhydryl)indole-2-carboxylate | HCID 54508530 | 95% |
Reaction Steps
Substantially the same procedure as in Reference Example 4 was repeated using 4-benzyloxybenzhydrol (30.0 g, 103 mmol) and ethyl indole-2-carboxylate (18.5 g, 97.9 mmol) to give 42.7 g (yield: 95%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05891902 |
| Source dataset | uspto-grants-1999_04 |
| ORD ID | ord-0529c54903954bfd8c50eca480c339c6 |
| Source note | uspto-grants-1999_04 |