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2-aminopropan-1-ol hydrochloride synthesis

2synthesis methods
-

Yield:6170-23-6 74%

Reaction Conditions:

Stage #1: 2,2,2-trichloro-acetimidic acid propyl esterwith N-iodo-succinimide in 1,2-dichloro-ethane at 110; for 3 h;Inert atmosphere;Sealed tube;
Stage #2: with hydrogenchloride in tetrahydrofuran;water;1,2-dichloro-ethane at 20; for 5 h;Inert atmosphere;Sealed tube;

References:

Mou, Xue-Qing;Chen, Xiang-Yu;Chen, Gong;He, Gang [Chemical Communications,2018,vol. 54,# 5,p. 515 - 518] Location in patent:supporting information