Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484674Generated: October 25, 2026

L-Threonine → HCID 178462331, compound

https://huagongshe.com/reaction/484674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-ThreonineHCID 6288—
ReactantSodium HydroxideHCID 14798—
Reactant2-Nitrobenzenesulfenyl chlorideHCID 24319—
ReactantPotassium bisulfateHCID 516920—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178462331HCID 178462331—

Reaction Steps

L-threonine (11.9 g) is added to dioxane (125 ml) and 2N sodium hydroxide (50 ml). To the vigorously stirred solution, o-nitrophenylsulfenyl chloride (20.9 g) is added in ten equal portions over fifteen minutes, while 2N sodium hydroxide (60 ml) is slowly added dropwise. After five more minutes the reaction mixture is diluted with water (400 ml) and acidified to pH 2.5 with 10% potassium bisulfate. The organic layer is immediately extracted with ethyl acetate (three 200 ml portions), and the combined extracts are dried over sodium sulfate, and then concentrated to an oil. The product crystallizes on scratching (20.0 g). Recrystallization of 17 g from acetone/hexane affords 9.5 g of crystals, melting point 145°-148° C. which are stored in a freezer and used promptly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04533660
Source datasetuspto-grants-1985_08
ORD IDord-e98c98c1543c45a58e965f9f8433e5b6
Source noteuspto-grants-1985_08