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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273073Generated: October 31, 2026

2-Propanol, 1-amino-2-methyl- → 2-Methyl-1-(tetrahydro-pyran-4-ylamino)-propan-2-ol

https://huagongshe.com/reaction/2273073

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Propanol, 1-amino-2-methyl-HCID 95102—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product2-Methyl-1-(tetrahydro-pyran-4-ylamino)-propan-2-olHCID 53534947—

Reaction Steps

2.75 g of 1-amino-2-methylpropan-2-ol are dissolved in 20 ml of MeOH. 1.71 ml of glacial acetic acid are added dropwise under an inert atmosphere. 2 g of tetrahydropyran-4-one in 10 ml of MeOH are added, the mixture is stirred for 30 minutes at room temperature and 1.98 g of sodium cyanoborohydride are added. The resulting mixture is stirred under an inert atmosphere for 15 hours. The reaction medium is poured into saturated aqueous NaHCO3 solution (100 ml). The resulting mixture is stirred for 30 minutes and then extracted with 4 times 100 ml of DCM. The organic phase is dried over Na2SO4, filtered and evaporated without heating. The MeOH contained in the aqueous phase is evaporated off and the extraction, drying, filtration and evaporation operation is repeated 3 times. 2.8 g of 2-methyl-1-((tetrahydro-2H-pyran-4-yl)amino)propan-2-ol are recovered in total.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120812B2
Source datasetuspto-grants-2015_09
ORD IDord-a9a91d309bf9476cb62b726e425cdcd1
Source noteuspto-grants-2015_09