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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430944Generated: October 30, 2026

Hydrochloric Acid → HCID 14503313, compound

https://huagongshe.com/reaction/430944

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 2.0 N 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 numberUS06656911B2
Source datasetuspto-grants-2003_12
ORD IDord-03a7a992e9a04e199ed1d599b6822d38
Source noteuspto-grants-2003_12