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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362185Generated: October 30, 2026

Hydrochloric Acid → HCID 14503313, compound

https://huagongshe.com/reaction/362185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAnisoleHCID 7519—
Reactant1,4-DioxaneHCID 31275—
Reactant3-(S)-[(benzyloxycarbonyl)amino]-2-acetoxy-4-methylpentanenitrileHCID 22871617—
ProductHCID 14503313HCID 1450331375%

Reaction Steps

To a solution containing 3-(S)-[(benzyloxycarbonyl)amino]-2-acetoxy-4-methylpentanenitrile (see example 1 of WO 96/16080) (15.2 g, 50.0 mmol) in 183 mL of dioxane was added 183 mL of concentrated hydrochloric acid and 7.45 mL of anisole. The reaction mixture was heated to reflux overnight. The hydrolysis reaction was allowed to cool to room temperature and then concentrated in vacuo. The resulting aqueous solution was extracted with ether (2×). The aqueous phase was placed on a Dowex 50X8-100 column (H+ form, preeluted with deionized water to pH=7). The column was eluted with 2.0N ammonium hydroxide and the pure fractions concentrated to afford 5.53 g (75%) of 3-(S)-amino-2-(R,S)-hydroxy-4-methylpentanoic acid as a pale yellow solid. FAB MS [M+H] m/z; Calcd: 148, Found: 148.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869455
Source datasetuspto-grants-1999_02
ORD IDord-56ebe0d20e0e4a49b72b431998a64173
Source noteuspto-grants-1999_02