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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815946Generated: October 30, 2026

(2R)-1-aminopropan-2-ol → HCID 11858494, compound

https://huagongshe.com/reaction/1815946

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R)-1-aminopropan-2-olHCID 439938—
Reactant4-(Benzyloxy)-2-fluorobenzonitrileHCID 11333628—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 11858494HCID 11858494—

Reaction Conditions

Temperature125 °C

Reaction Steps

A solution of (R)-(−)-1-amino-propan-2-ol (389 g, 5.19 mol) in dimethyl sulfoxide (600 mL) was added to a solution of the product from Step A (786 g, 3.46 mol), basic alumina (786 g), and 4 Å molecular sieves (131 g). The stirred mixture was heated at 110-140° C. for 24 h, cooled and filtered, the filter-aide was washed with 10 L of 4:1 ether-ethyl acetate followed by 4 L of 3:2 ethyl acetate-hexane. The organic washes were extracted with water (5 L) and the aqueous phase was extracted with 25% ethyl acetate-hexane (4×2 L). The combined organic phases were washed with water and brine, dried over sodium sulfate, concentrated to about 3 L and allowed to stand for 48 h. The precipitated solid was collected by filtration, washed with hexane, and vacuum-dried to provide the desired product in two crops (619 g and 86 g). The concentated supernatant was applied to a 5 kg silica gel pad and eluted with a gradient of 10-50% ethyl acetate-hexane to give, after concentration in vacuo, additional product (119 g): total yield was 791 g (81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881749B2
Source datasetuspto-grants-2005_04
ORD IDord-2dc3b9ab708549d8b7361e969c2d6e4f
Source noteuspto-grants-2005_04