HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 5-Bromoindole-2-carboxylate → (5-Bromo-1H-indol-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 5-Bromoindole-2-carboxylate | HCID 259091 | — |
| Reactant | Aluminum;lithium | HCID 16211445 | — |
| Product | (5-Bromo-1H-indol-2-yl)methanol | HCID 13567955 | — |
Reaction Steps
The title compound was prepared from ethyl 5-bromo-1H-indole-2-carboxylate and lithium aluminum in substantially the same manner, as described in step 3 of Example 1. The product was obtained as a solid; mp: 111-112° C. Mass spectrum (ESI, [M−H]−) m/z 224. 1H NMR (400 MHz, DMSO-d6) δ 7.62 (s, 1H), 7.27 (d, 1H, J =8.02 Hz), 7.12 (d, 1H, J=8.02 Hz), 6.25 (s, 1H), 5.29 (t, 1H, J=5.50 Hz), 4.59 ppm (d, 2H, J=5.6 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07459478B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-36a5c85fc597489a88295bb834672bea |
| Source note | uspto-grants-2008_12 |