HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638772Generated: October 30, 2026
Ammonia → N,N-Dimethyl-3,4-dioleyloxybenzylamine
https://huagongshe.com/reaction/638772
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3,4-Dioleyloxybenzaldehyde | HCID 16103016 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N,N-Dimethyl-3,4-dioleyloxybenzylamine | HCID 23642188 | — |
Reaction Steps
To a solution of triethylamineamine (2.0 mL, 14 mmol) in ethanol (20 mL) was added dimethylamine hydrochloride (1.63 g, 20 mmol), titanium tetraisopropoxide (5.96 mL, 20 mmol) and 3,4-dioleyloxybenzaldehyde (6.39 g, 10 mmol). The mixture was allowed to stir under argon for 10 h at room temperature. Sodium borohydride (0.57 g, 15 mmol) was added to the reaction mixture which was then allowed to stir at room temperature overnight. Concentrated aqueous ammonia (4 mL) was added slowly to the reaction mixture. The reaction mixture was filtered and the solids washed with dichloromethane. The filtrate was dried over K2CO3, filtered and concentrated. The resultant oil was purified via flash chromatography (2-10% acetone in dichloromethane, 0.5% TEA gradient) to afford 5.81 g (87-+%) of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691405B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-3ed07e4e92d04d8fa9dd75535ac37a43 |
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| Source note | uspto-grants-2010_04 |
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