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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951243Generated: November 3, 2026

Sodium Thiosulfate → Tert-butyl 3-methyl-1-oxobutan-2-ylcarbamate

https://huagongshe.com/reaction/1951243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl N-[(2S)-1-hydroxy-3-methylbutan-2-yl]carbamateHCID 7021464—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 3-methyl-1-oxobutan-2-ylcarbamateHCID 545985—

Reaction Steps

To a solution of Dess-Martin periodinane (3.12 g, 0.0073 mol, 1.5 eq) in dichloromethane (25 mL) was added a solution of N-Boc-L-valinol (1 g, 0.0049 mol, 1 eq) in dichloromethane (25 mL). The reaction mixture was stirred at room temperature for 3 h and was diluted with diethyl ether (50 mL). The mixture was poured into an aqueous saturated solution of sodium bicarbonate (100 mL) containing sodium thiosulfate (8.16 g, 10.5 eq). The mixture was stirred for 30 min and the layers were separated. The ether layer was washed with an aqueous saturated solution of sodium bicarbonate (50 mL), water (50 mL), dried (sodium sulfate) and filtered. The filtrate was concentrated to give the crude (1-formyl-2-methyl-propyl)-carbamic acid tert-butyl ester used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404693B2
Source datasetuspto-grants-2013_03
ORD IDord-84d75cb4f1aa49e59b2d30e6c39fd674
Source noteuspto-grants-2013_03