HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870167Generated: October 26, 2026
Sodium borohydride → 2-((2,4-Dichlorobenzyl)(methyl)amino)-1-(3-nitrophenyl)ethanol
https://huagongshe.com/reaction/870167
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-((2,4-Dichlorobenzyl)(methyl)amino)-1-(3-nitrophenyl)ethanone | HCID 67455430 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-((2,4-Dichlorobenzyl)(methyl)amino)-1-(3-nitrophenyl)ethanol | HCID 67455496 | — |
Reaction Steps
Into a 500-mL 3-necked round-bottom flask, was placed a solution of 2-((2,4-dichlorobenzyl)(methyl)amino)-1-(3-nitrophenyl)ethanone (28 g, 1.00 equiv, Crude) in methanol (280 mL), NaBH4 (6.38 mg, 0.17 mmol, 2.00 equiv). The resulting solution was stirred for 0.5 h at 0° C. The reaction progress was monitored by LCMS. The reaction was then quenched by the addition of 10 mL of acetone. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:10˜1:5). This resulted in 14 g of 2-((2,4-dichlorobenzyl)(methyl)amino)-1-(3-nitrophenyl)ethanol as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969377B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-9bb81c1397a341d7b70ba494d9286de1 |
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| Source note | uspto-grants-2015_03 |
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