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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905326Generated: November 1, 2026

Benzyl Alcohol → (2RS, 3S)-3-carbobenzoxyamino-2-hydroxy-5-methylhexyl benzyl ether

https://huagongshe.com/reaction/1905326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactant(3S)-3-carbobenzoxyamino-5-methyl-1,2-epoxyhexaneHCID 13909433—
Product(2RS, 3S)-3-carbobenzoxyamino-2-hydroxy-5-methylhexyl benzyl etherHCID 131715984—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 100 mg of (3S)-3-carbobenzoxyamino-5-methyl-1,2-epoxyhexane, 2 g of dry silica gel and 2 ml of benzyl alcohol was heated at 100° C. for 16 hours. After filtration of the silica gel, the filtrate was evaporated under reduced pressure to obtain 105 mg of (2RS, 3S)-3-carbobenzoxyamino-2-hydroxy-5-methylhexyl benzyl ether as a colorless oil. To a solution of 86 mg of the ether obtained in 10 ml of methanol was added 0.14 ml of a 2N-hydrochloric acid, and the mixture was hydrogenated over 17 mg of palladium charcoal under hydrogen atmosphere. After filtration of the catalyst, 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 17 mg of (2RS, 3S)-3-amino-2-hydroxy-5-methylhexyl benzyl ether hydrochloride as a colorless viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04841067
Source datasetuspto-grants-1989_06
ORD IDord-7ec00e42a77a45268ff6e7a5b7a932e3
Source noteuspto-grants-1989_06