HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725241Generated: November 1, 2026
Borane → Butyl[(2,3-dimethoxyphenyl)methyl]amine
https://huagongshe.com/reaction/1725241
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Borane | HCID 6331 | — |
| Reactant | N-butyl-2,3-dimethoxybenzamide | HCID 347459 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Butyl[(2,3-dimethoxyphenyl)methyl]amine | HCID 4717318 | 54.3% |
Reaction Steps
N-Butyl-2,3-dimethoxybenzamide (5.37 g, 22.6 mmol) was dissolved in freshly distilled THF (230 mL) and cooled in an ice bath under an argon atmosphere. Borane (28 mL of a 2 M solution of the dimethylsulfide complex in diethyl ether) was added and the ice bath was removed after 15 minutes. The reaction mixture was refluxed overnight and was then allowed to cool to room temperature. The reaction was quenched by careful addition of 10% HCl (11 mL) and the mixture was stirred for four hours and then concentrated in vacuo. The residue was taken up in ethyl acetate (300 mL) and washed with aqueous 2 M K2CO3 (3×100 mL), and brine (100 mL), dried over Na2SO4, and concentrated in vacuo. Purification on silica gel (160 g) with ethyl acetate (33-100% gradient) in heptane and finally 5% ethanol in ethyl acetate as the eluent yielded 2.74 g (54%) of a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07488844B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-a3db7ae055174b3597fcde40db085e0d |
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| Source note | uspto-grants-2009_02 |
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