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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905330Generated: November 1, 2026

Benzylamine → (3S)-N-benzyl-3-carbobenzoxyamino-2-hydroxy-5-methylhexylamine

https://huagongshe.com/reaction/1905330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant(3S)-3-carbobenzoxyamino-5-methyl-1,2-epoxyhexaneHCID 13909433—
SolventDiethyl EtherHCID 3283—
Product(3S)-N-benzyl-3-carbobenzoxyamino-2-hydroxy-5-methylhexylamineHCID 56634722—

Reaction Steps

To a solution of 100 mg of (3S)-3-carbobenzoxyamino-5-methyl-1,2-epoxyhexane in 10 ml of diethyl ether were added 2 g of dry silica gel and 0.1 ml of benzylamine, and the mixture was stirred for 16 hours at room temperature, then heated under reflux for 2 hours. After filtration of the silica gel, the filtrate was evaporated under reduced pressure. The residue was purified by preparative silica gel thin layer chromatography (developing solvent: lower layer of chloroform/methanol/water=8/3/1 by volume) to obtain 56 mg of (3S)-N-benzyl-3-carbobenzoxyamino-2-hydroxy-5-methylhexylamine as a colorless viscous oil. To a solution of 54 mg of the amine compound obtained in 10 ml methanol was added 0.2 ml of a 2N-hydrochloric acid. The mixture was hydrogenated over 10 mg of palladium charcoal under hydrogen atmosphere. After filtration of the catalyst, the filtrate was evaporated under reduced pressure to obtain 43 mg of (3S) -N-benzyl-3-amino-2-hydroxy-5-methylhexylamine dihydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04841067
Source datasetuspto-grants-1989_06
ORD IDord-c447ce8d557047cc936407ae1553d763
Source noteuspto-grants-1989_06