HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660050Generated: October 27, 2026
Ammonia → 1-(3,4-Dimethylphenyl)ethan-1-amine
https://huagongshe.com/reaction/660050
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 3,4-Dimethylacetophenone | HCID 77193 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Catalyst | Titanium n-propoxide | HCID 4379755 | — |
| Solvent | Ethylacetate methanol | HCID 21584119 | — |
| Product | 1-(3,4-Dimethylphenyl)ethan-1-amine | HCID 5086468 | 18% |
Reaction Steps
16.4 ml (150.0 mmol) of tetrapropyl orthotitanate were added to a solution of 4.46 g (30.0 mmol) of 3,4-dimethylacetophenone in a 2 M ethanolic ammonia solution (75 ml), and the mixture was stirred for 6 hours at RT. 1.7 g (45.0 mmol) of sodium borohydride were then added, and stirring was continued for a further 16 hours at RT. Thereafter, the reaction solution was poured into a saturated aqueous ammonia solution (75 ml). The precipitate that formed was filtered off with suction, and then washing with ethyl acetate was carried out. The aqueous filtrate was concentrated in vacuo, followed by extraction twice with ethyl acetate. The combined ethyl acetate phases were extracted three times with 2 M hydrochloric acid. The combined aqueous phases were adjusted to pH 11 with a 2 M aq. NaOH solution and then extracted three times with ethyl acetate. The combined organic phases were dried over MgSO4, filtered and concentrated in vacuo. CC (ethyl acetate/MeOH 9:1) yielded 799 mg (5.4 mmol, 18%) of 1-(3,4-dimethylphenyl)ethylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084470B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-ba02396c21e84cc49b866231a613e00b |
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| Source note | uspto-grants-2011_12 |
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