HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → Methyl 4-[5-(2-hydroxyethyl)-1-propylindol-3-ylmethyl]-3-methoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 4-[5-(formylmethyl)-1-propylindol-3-ylmethyl]-3-methoxybenzoate | HCID 19994986 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-[5-(2-hydroxyethyl)-1-propylindol-3-ylmethyl]-3-methoxybenzoate | HCID 19994996 | 65% |
Reaction Steps
Sodium borohydride (0.027 g) was added to a stirred solution of methyl 4-[5-(formylmethyl)-1-propylindol-3-ylmethyl]-3-methoxybenzoate (0.54 g) in methanol (15 ml) under a nitrogen atmosphere. After 30 min, the solvent was evaporated. The residue was dissolved in ethyl acetate, washed with water (twice), brine, and then dried (MgSO4) and evaporated. The product was purified by flash chromatography, eluting with 7:3 hexane:ethyl acetate, to give methyl 4-[5-(2-hydroxyethyl)-1-propylindol-3-ylmethyl]-3-methoxybenzoate (0.35 g, 65%) as an oil: partial NMR (300 MHz, DMSO-d6): 0.80(t, 3H, CH3), 1.70(m, 2H, CH2), 2.74(t, 2H, CH2), 3.56(t, 2H, CH2), 3.83(s, 3H, OCH3), 3.91(s, 3H, OCH3), 4.03(m, 4H, NCH2, ArCH2Ar').
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041460 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-8340c86303114426909084b842b00ec9 |
| Source note | uspto-grants-1991_08 |