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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant3,4-DimethylacetophenoneHCID 77193—
ReactantSodium borohydrideHCID 4311764—
CatalystTitanium n-propoxideHCID 4379755—
SolventEthylacetate methanolHCID 21584119—
Product1-(3,4-Dimethylphenyl)ethan-1-amineHCID 508646818%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084470B2
Source datasetuspto-grants-2011_12
ORD IDord-ba02396c21e84cc49b866231a613e00b
Source noteuspto-grants-2011_12