HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111922Generated: November 2, 2026
2-Benzofurancarboxaldehyde → HCID 68575168, compound
https://huagongshe.com/reaction/2111922
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Benzofurancarboxaldehyde | HCID 61341 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 43652145 | HCID 43652145 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68575168 | HCID 68575168 | 105.4% |
Reaction Steps
Sodium triacetoxyborohydride (0.88 g, 4.16 mmol) is added to a stirred solution of 4-(3-methyl-butylamino)-piperidine-1-carboxylic acid tert-butyl ester (0.75 g, 2.77 mmol), benzofuran-2-carboxaldehyde (0.50 g, 3.46 mmol), and dichloromethane (14 ml). The reaction is stirred overnight at room temperature under nitrogen. The reaction is poured into aqueous saturated NaHCO3 (50 ml) and extracted with dichloromethane (25 ml×3). The organic layer is washed with aqueous saturated NaHCO3 and dried over Na2SO4, and filtered. The crude product is concentrated on a rotary evaporator and purified by flash chromatography on silica gel eluting with 0-30% (1:2 (10% NH4OH in methanol):ethanol) to yield (1.17 g) of 4-{[(benzofuran-2-yl)methyl]-(3-methylbutyl)-amino}-piperidine-1-carboxylic acid tert-butyl ester: mass spectrum (ion spray): m/z=401 (M+1); 1H NMR (CDCl3): δ=7.57-7.41 (2H, m), 7.30-7.16 (2H, m), 6.55 (1H, s), 4.15 (2H, brs), 3.81 (2H, s), 2.75-2.56 (6H, m), 1.80 (2H, brd), 1.63-1.53 (3H, m), 1.46 (9H, s), 1.42-1.33 (1H, m), 0.92-0.85 (6H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07521462B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-6e0c4636e2544f7c9137b0c59baf6d62 |
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| Source note | uspto-grants-2009_04 |
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