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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935401Generated: October 31, 2026

Potassium bisulfate → (S)-tert-butyl 1-oxohexan-2-ylcarbamate

https://huagongshe.com/reaction/1935401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bisulfateHCID 516920—
Reactanttert-butyl (1S)-1-{[methoxy(methyl)amino]carbonyl}pentylcarbamateHCID 10061913—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product(S)-tert-butyl 1-oxohexan-2-ylcarbamateHCID 10420833—

Reaction Conditions

Temperature5 °C

Reaction Steps

A mechanically stirred suspension of lithium aluminum hydride (5.00 g, 0.131 mol) in ether (250 mL) was cooled to −45“C under nitrogen. A solution of the product from Step A (28.3 g, 0.103 mol) in ether (125 mL) was added, maintaining the temperature below −35° C. when the addition was complete, the reaction was warmed to 5° C., then recooled to −45° C. A solution of potassium hydrogen sulfate (27.3 g, 0.200 mol) in water was slowly added, maintaining the temperature below −5° C. After quenching, the reaction was stirred at room temperature for 1 h. The mixture was filtered through Celite, the ether evaporated, and the remainder partitioned between ethyl acetate and 2% potassium hydrogen sulfate. After washing with saturated brine, drying over magnesium sulfate and solvent removal, the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06387903B1
Source datasetuspto-grants-2002_05
ORD IDord-ab91bc18cb264d949da2a990b6a451e5
Source noteuspto-grants-2002_05