HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490402Generated: October 29, 2026
4-Aminobiphenyl → 4-(Biphenyl-4-ylaminomethyl)-5-methyl-furan-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/490402
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminobiphenyl | HCID 7102 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Methyl 4-formyl-5-methylfuran-2-carboxylate | HCID 15503958 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(Biphenyl-4-ylaminomethyl)-5-methyl-furan-2-carboxylic acid methyl ester | HCID 58824195 | 29.1% |
Reaction Steps
A solution of biphenyl-4-ylamine (150 mg, 0.883 mmoles) and 4-formyl-5-methyl-furan-2-carboxylic acid methyl ester (157) (135 mg, 0.803 mmoles) in methanol (2.0 ml) was stirred over molecular sieves (type 3 Å) for 1 hour. Sodium cyanoborohydride (55 mg, 0.883 mmoles) was added and the mixture stirred for 18 hour at room temperature. The mixture was concentrated and partitioned between ethyl acetate (25 ml) and saturated aqueous sodium bicarbonate (30 ml). The aqueous phase was re-extracted with ethyl acetate (2×25 ml) and the combined extracts were washed with brine (50 ml) and dried (MgSO4). After removal of the solvent, the residue was purified by flash chromatography, using a gradient elution of petrol/diethyl ether 9:1 v/v to 4:1 v/v, to afford compound 158 (75 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528157B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-e4a8d784714646a69b3331672d9e5c52 |
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| Source note | uspto-grants-2009_05 |
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