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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245896Generated: November 2, 2026

Isopropanol → HCID 23091320, compound

https://huagongshe.com/reaction/2245896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 23091182HCID 23091182—
SolventEthanolHCID 702—
ProductHCID 23091320HCID 23091320—

Reaction Conditions

Temperature50 °C

Reaction Steps

180 mL of isopropanol and 180 mL of ethanol were added to 36.0 g of the 1-(trifluoroacetylamino)-1-(1-naphthyl)-2-methyl-2-propanol obtained, and 63 g of an aqueous solution of 22% by weight of potassium hydroxide was added dropwise thereto over 30 minutes at room temperature. The inner temperature of the mixture was raised to 50° C. and, at the same temperature, the mixture was stirred for 2 hours to effect reaction. The reaction mixture was concentrated, and 500 mL of chloroform and 180 mL of water were added to the resulting concentrated residue to carry out extraction treatment. The organic layer obtained was washed with 100 mL of water and the organic layer obtained was dried over dehydrated sodium sulfate and then concentrated. The resulting concentrated residue was dried at an inner temperature of 30° C. under reduced pressure to obtain 28.0 g of brown, viscous and oily 1-amino-1-(1-naphthyl)-2-methyl-2-propanol

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683215B2
Source datasetuspto-grants-2010_03
ORD IDord-06e2e507658e4c47a6f5beea8e5a6e10
Source noteuspto-grants-2010_03