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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981105Generated: October 29, 2026

L-Valine → N-(tert-Butylcarbamoyl)-L-valine

https://huagongshe.com/reaction/1981105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-ValineHCID 6287—
Reactanttert-Butyl isocyanateHCID 62412—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
ProductN-(tert-Butylcarbamoyl)-L-valineHCID 2850876376.2%

Reaction Steps

4.69 g of L-valine was dissolved in 40 ml of a 1N sodium hydroxide aqueous solution, and 5 ml of tetrahydrofuran was added to the solution. While stirring, 4.00 g of tert-butyl isocyanate was added, and the stirring was continued overnight at room temperature. After 10 ml of a 1N sodium hydroxide aqueous solution was added to the reaction mixture, the mixture was washed twice with 50 ml of ethyl acetate and acidified with 6N hydrochloric acid. Then, the reaction mixture was extracted twice with 100 ml of ethyl acetate. The extracts were washed twice with 50 ml of a saturated sodium chloride aqueous solution. After drying over anhydrous sodium sulfate and then concentrating under reduced pressure, recrystallization was carried out from an ethyl acetate-hexane mixture to obtain 6.6 g of N-tert-butylcarbamoyl-L-valine as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04512898
Source datasetuspto-grants-1985_04
ORD IDord-b7066bfbacfc4e73bf0d972a9eb0696a
Source noteuspto-grants-1985_04