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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | (3S)-3-carbobenzoxyamino-5-methyl-1,2-epoxyhexane | HCID 13909433 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (3S)-N-benzyl-3-carbobenzoxyamino-2-hydroxy-5-methylhexylamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04841067 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-c447ce8d557047cc936407ae1553d763 |
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| Source note | uspto-grants-1989_06 |
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