HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 6-chloroindole-2-carboxylate → (6-Chloro-1H-indol-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 6-chloroindole-2-carboxylate | HCID 7015027 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-Chloro-1H-indol-2-yl)methanol | HCID 16115151 | 111.7% |
Reaction Steps
To 6-chloro-1H-indole-2-carboxylic acid ethyl ester (8.57 g) in THF at 0° C. was added lithium aluminum hydride solution (1M, in THF) dropwise and the reaction mixture was stirred for 3.5 h. The mixture was quenched with H2O, 15% NaOH, and H2O before it was filtered and rinsed with THF. Evaporation of the solvent gave 7.77 g of the crude (6-Chloro-1H-indol-2-yl)-methanol which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06635771B2 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-3dbe040d188f412eb371b065317d254c |
| Source note | uspto-grants-2003_10 |