HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → Ethyl 4-[3-(3-nitrobenzyl)indol-1-yl]butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 4-[3-(3-nitrobenzoyl)indol-1-yl]butyrate | HCID 10547793 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-[3-(3-nitrobenzyl)indol-1-yl]butyrate | HCID 19024737 | 35.9% |
Reaction Steps
To a solution of ethyl 4-[3-(3-nitrobenzoyl)indol-1-yl]butyrate (0.5 g) in tetrahydrofuran (10 ml) were added sodium borohydride (99.4 mg) and boron trifluoride etherate (0.485 ml) at -25° C., and the mixture was stirred at the same temperature for 2 hours. The mixture was poured into a mixture of ethyl acetate and ice water. The organic layer was separated, washed with water and brine, and dried over magnesium sulfate. After evaporation of the solvent, the residue was chromatographed on silica gel (25 g) eluting with a mixture of ethyl acetate and hexane (1:4) to give ethyl 4-[3-(3-nitrobenzyl)indol-1-yl]butyrate (173 mg) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05212320 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-d5b05f02ad3247ef84eb4ad05375a1f2 |
| Source note | uspto-grants-1993_05 |