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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442648Generated: October 30, 2026

Benzyl chloroformate → HCID 131720810, compound

https://huagongshe.com/reaction/442648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantHCID 14503313HCID 14503313—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 131720810HCID 13172081092%

Reaction Steps

To a solution under an atmosphere of nitrogen containing 1.0 g (6.8 mmol) of 3-(S)-amino-2-(R,S)-hydroxy-4-methylpentanoic acid in 9.5 mL of 1N NaOH and 10 mL of dioxane was added 1.43 g (8.4 mmol) of benzyl chloroformate. The pH was maintained above pH 8 with 1N NaOH as needed. The reaction mixture was allowed to stir at room temperature overnight. The reaction was diluted with water and washed with ether. The aqueous layer was acidified with 1N HCl to pH=2 and extracted with ether (2×). The combined organic layers were dried over magnesium sulfate, filtered and evaporated in vacuo to afford 1.75 g (92%) of 3-(S)-[(benzyloxycarbonyl)amino]-2-(R,S)-hydroxy-4-methylpentanoic acid as a light yellow viscous oil. FAB MS [M+H] m/z; Calcd: 282, Found: 282.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891852
Source datasetuspto-grants-1999_04
ORD IDord-8e0a86ed076b4972bbb5214faa663d05
Source noteuspto-grants-1999_04