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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242549Generated: October 30, 2026

Isopropanol → HCID 23091158, compound

https://huagongshe.com/reaction/2242549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 23091235HCID 23091235—
SolventEthanolHCID 702—
ProductHCID 23091158HCID 2309115897%

Reaction Conditions

Temperature50 °C

Reaction Steps

After 170 mL of isopropanol and 170 mL of ethanol were added to 36.0 g of the 1-(trifluoroacetylamino)-1-(2-naphthyl)-2-methyl-2-propanol obtained, 56 g of an aqueous solution of 22% by weight of potassium hydroxide was added dropwise thereto over 30 minutes at room temperature. Then, 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 320 mL of chloroform and 160 mL of water were added to the resulting concentrated residue to carry out extraction treatment. The organic layer obtained was washed with 80 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 24.3 g of a brown solid of 1-amino-1-(2-naphthyl)-2-methyl-2-propanol (yield: 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671213B2
Source datasetuspto-grants-2010_03
ORD IDord-931a544c571147d9876efd7aad025862
Source noteuspto-grants-2010_03