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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294584Generated: October 29, 2026

Dichloromethane → rac-(1R,2R)-2-(methylamino)cyclohexan-1-ol

https://huagongshe.com/reaction/1294584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
Reactant(1r, 2r)-2-Methylamino cyclohexanol (r)-mandelic acid saltHCID 131726521—
SolventWaterHCID 962—
SolventSodium chloride; waterHCID 57417360—
Productrac-(1R,2R)-2-(methylamino)cyclohexan-1-olHCID 1284719397.4%

Reaction Steps

NaOH (108 g, 2.69 mol) was dissolved in water (350 ml). Brine (400 ml) was added and cooled to room temperature. Dichloromethane (300 ml) and (1R, 2R)-2-methylamino cyclohexanol (R)-mandelic acid salt (151.5 g, 538 mmol) were added and the mixture was stirred vigorously for 10 min. The layers were separated and the aqueous layer was again extracted with dichloromethane (3×200 ml). (separation of the layers is a time consuming process). The combined dichloromethane layers were dried (Na2SO4) and concentrated to give an oil (67.7 g, 97% yield). This oil was combined with two other batches of 2.3 g and 6.4 g (both with e.e.=99+%) and purified by Kugelrohr distillation (p=0.5 mbar, T=80-90° C.) giving a colorless oil (72.0 g, 92%) with 94% purity according to GC. This oil was again Kugelrohr distilled (p=0.3 mbar) giving two product containing fractions:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241770B2
Source datasetuspto-grants-2007_07
ORD IDord-0995a492aee34744b35775fd16da17fa
Source noteuspto-grants-2007_07