HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067837Generated: November 2, 2026
Sodium borohydride → Ethyl 4-chloro-6-[4-(hydroxymethyl)phenoxy]-1-methyl-2-indolecarboxylate
https://huagongshe.com/reaction/1067837
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 4-chloro-6-(4-formylphenoxy)-1-methyl-2-indolecarboxylate | HCID 21194191 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-chloro-6-[4-(hydroxymethyl)phenoxy]-1-methyl-2-indolecarboxylate | HCID 21194045 | 100.4% |
Reaction Steps
A mixture of 0.90 g (2.52 mmol) of ethyl 4-chloro-6-[4-formylphenoxy)-1-methyl-2-indolecarboxylate, 0.10 g (2.52 mmol) of sodium borohydride and 20 ml of ethanol was stirred at 0° C. for 2 hours. The reaction mixture was poured onto ice water. The resulting mixture was then extracted three times with ethyl acetate. The combined extracts were washed with saturated sodium chloride aqueous solution. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure to give 0.91 g (>99%) of ethyl 4-chloro-6-[4-(hydroxymethyl)phenoxy]-1-methyl-2-indolecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06248772B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-649eb4e8e0bf4abaa87cb28f49e40fd4 |
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| Source note | uspto-grants-2001_06 |
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