HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methyl-1H-indole-4-carbaldehyde → alpha-(2-methoxyphenyl)-1-methyl-1H-indol-4-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methyl-1H-indole-4-carbaldehyde | HCID 17221111 | — |
| Reactant | 2-Bromo anisole magnesium | HCID 66862467 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | alpha-(2-methoxyphenyl)-1-methyl-1H-indol-4-methanol | HCID 19800111 | — |
Reaction Steps
Using the procedure of Step B of Example 1, 36.8 g of the product of Step A and 104 ml of a solution of 2-bromo anisole magnesium compound in tetrahydrofuran titrating 1.94N were reacted. Extraction was carried out with ethyl acetate and the extracts were washed with salt water and brought to dryness. The residue was chromatographed on silica (eluant: methylene chloride) to obtain 46.S B of the expected product melting at 95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05182282 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-401a1b3e0b7541e2a2887232a41ba8d4 |
| Source note | uspto-grants-1993_01 |