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(1-amino-3-phenylpropan-2-yl)(methyl)amine synthesis

2synthesis methods
-

Yield:-

Reaction Conditions:

with LiAlH4;sodium carbonate in tetrahydrofuran;water;

Steps:

17.25.3 (3)

(3) 1-Amino-(S)-2-N-Methylamino-3-Phenylpropane There was added 10 mmoles (2.36 grams) of N-ethyloxycarbonyl-(L)-phenylalanineamide (produced from (L)-phenylalanineamide and ethyl chloroformate in the presence of Na2 CO3 in an ice bath) in small portions to an ice cooled suspension of 90 mmoles (3.41 grams) of LiAlH4 in 110 ml of tetrahydrofuran. The mixture was heated at reflux for 24 hours. Hydrolysis was carried out under ice ooling with 360 mmoles (6.50 ml) of water. Further working up was analogous to (a). The product was distilled in a high vacuum (10-4 Torr) at 75° C. air bath temperature. Colorless liquid, M.P. of the hydrochloride 160° C.

References:

US4704464,1987,A