HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-methoxy-2-methyl-1-(phenylmethyl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-methoxy-2-methyl-1H-indole | HCID 10773274 | — |
| Catalyst | Benzyl Bromide | HCID 7498 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-methoxy-2-methyl-1-(phenylmethyl)-1H-indole | HCID 10777147 | 84% |
Reaction Steps
4-Methoxy-2-methyl-1H-indole (1 g, 6.2 mmol) was added to 248 mg (6.2 mmol) of 60% sodium hydride/mineral oil (washed with hexane before adding DMF) in 15 mL of DMF and after stirring for 0.5 hour, 0.74 mL (6.2 nmol) of benzyl bromide was added. The mixture was stirred at room temperature for 18 hours, diluted with water and extracted with ethyl acetate. The ethyl acetate solution was washed with brine, dried (MgSO4) and after concentrating at reduced pressure, the residue was chromatographed on silica gel eluting with 20% EtOAc/hexane to give 1.3 g(84% yield) of 4-methoxy-2-methyl-1-(phenylmethyl)-1H-indole, melting at 96-116° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06175021B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-2188d1fd16544025ae24d761b5795a20 |
| Source note | uspto-grants-2001_01 |