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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368058Generated: November 2, 2026

Water → tert-Butyl [(1S)-1-methyl-2-(pyridin-4-yloxy)ethyl]carbamate

https://huagongshe.com/reaction/2368058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant(S)-2-((tert-butoxycarbonyl)amino)propyl 4-methylbenzenesulfonateHCID 13200311—
ReactantHCID 178418642HCID 178418642—
SolventDimethylformamideHCID 6228—
Producttert-Butyl [(1S)-1-methyl-2-(pyridin-4-yloxy)ethyl]carbamateHCID 5751747820.7%

Reaction Steps

To a suspension of sodium hydride (oil, 60%, 1.61 g) in DMF (50 mL) was added 4-hydroxypyridine (3.83 g) under ice-cooling. The reaction mixture was stirred for 30 min under ice-cooling, and (2S)-2-[(tert-butoxycarbonyl)amino]propyl 4-methylbenzenesulfonate (13.3 g) was added thereto in small portions under ice-cooling. The reaction mixture was stirred for 2 hr under ice-cooling, and at 60° C. for 3 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (2.10 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703758B2
Source datasetuspto-grants-2014_04
ORD IDord-48c3b04b55f444838f6783b89dbd48f3
Source noteuspto-grants-2014_04