Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List 2-NAPHTHALEN-2-YL-ETHYLAMINE
2017-68-7

2-NAPHTHALEN-2-YL-ETHYLAMINE synthesis

4synthesis methods
-

Yield:2017-68-7 67%

Reaction Conditions:

with aluminium trichloride in water

Steps:

2.A 2-naphthaleneethanamine
Step A 2-naphthaleneethanamine Aluminum trichloride (7.6 g, 57 mmole) was added in portions to 30 mL of ether cooled to 0° C. under nitrogen. In a separate flask, lithium aluminum hydride (2.2 g, 57 mmole) was slurried in 30 mL of ether and cooled to -5° C. with an ice/acetone bath. The etherial aluminum trichloride solution was added dropwise to the LiAlH4 slurry at such a rate as to maintain a temperature of 0° C. Fifteen minutes after addition was complete, 2-naphthylacetonitrile (4.0 g, 24 mmole) in 40 mL of ether was added dropwise while maintaining a temperature of 0° C. The reaction mixture was stirred for an additional 15 minutes at 0° C. and then allowed to warm to room temperature for 1 hour. After recooling to 0° C., the reaction was quenched by careful dropwise addition of water. The mixture was diluted with ether, partitioned, and the aqueous phase was basified with 30% NH4 OH solution. Extraction of the aqueous phase with ether, combination of the organic phases, drying, and concentration gave a colorless oil (2.7g, 67% yield). 1 H MNR (CDCl3): δ 7.80 (m, 3H), 7.65 (s, 1H), 7.45 (m, 2H), 7.30 (m, 1H), 3.06 (t, 2H), 2.91 (t, 2H), 1.35 (s, 2H).

References:

E. I. Du Pont de Nemours and Company US5378708, 1995, A

FullText

2-NAPHTHALEN-2-YL-ETHYLAMINE Related Search: