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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644024Generated: November 1, 2026

Hydrochloric Acid → (2R)-1-methoxy-4-methyl-pentan-2-amine

https://huagongshe.com/reaction/1644024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant(R)-2-(1-methoxy-4-methylpentan-2-yl)isoindoline-1,3-dioneHCID 66772667—
SolventMethanolHCID 887—
Product(2R)-1-methoxy-4-methyl-pentan-2-amineHCID 8659756677.5%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of (R)-2-(1-methoxy-4-methylpentan-2-yl)isoindoline-1,3-dione (example 9b) (3.87 g, 14.84 mmol) in methanol (30 mL), was added hydrazine hydrate (0.866 ml, 17.81 mmol) and the reaction mixture was warmed up to 45° C. for about 3 hours. The mixture was acidified with 2N HCl and stirred at 45° C. for 30 min. The solution was cooled to room temperature, filtered and evaporated. The residue was taken up with 2N NaOH and extracted with ether, dried over MgSO4, filtered and evaporated to give 1.51 g of (R)-1-methoxy-4-methylpentan-2-amine. Yield 77%. 1H NMR (500 MHz, CDCl3): δ 0.91 (m, 6H); 1.17 (m, 2H); 1.58 (s, 2H); 1.71 (m, 1H); 3.02 (m, 1H); 3.10 (m, 1H); 3.32 (m, 1H); 3.35 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124121B2
Source datasetuspto-grants-2012_02
ORD IDord-59f834f3759047ce90ee3964bf78b8f6
Source noteuspto-grants-2012_02