232597-44-3

Usage

Uses

Used in Pharmaceutical Industry:
1-(4-BOC-AMINO-PHENYL)-ETHANOL is used as a building block for the synthesis of various pharmaceutical compounds. Its presence of a BOC protecting group allows for the creation of amine-protected intermediates, which are crucial in the development of new drugs and medications.
Used in Organic Synthesis:
1-(4-BOC-AMINO-PHENYL)-ETHANOL is used as a reagent in the manufacture of other organic compounds. Its versatility in protecting amine groups makes it a valuable asset in the synthesis of a wide range of organic molecules, contributing to the advancement of chemical research and development.

InChI:InChI=1/C13H19NO3/c1-9(15)10-5-7-11(8-6-10)14-12(16)17-13(2,3)4/h5-9,15H,1-4H3,(H,14,16)

Upstream product

• 232597-42-1 tert-butyl 4-acetylphenylcarbamate 
• 57295-14-4 tert-butyl 4-vinylphenylcarbamate 

Downstream Products

• 1286240-16-1 (R)-1-(N-Boc-4-aminophenyl)ethyl acetate 

Relevant academic research and scientific papers

Conversion of Olefins into Ketones by an Iron-Catalyzed Wacker-type Oxidation Using Oxygen as the Sole Oxidant

We describe a mild and operationally simple procedure for the oxidation of olefins into ketones. The reaction is catalyzed by the hexadecafluorinated iron–phthalocyanine complex FePcF16 with stoichiometric amounts of triethylsilane as an additive under oxygen atmosphere to give ketones in good to high yields with excellent chemoselectivity and functional group tolerance. Ketone formation proceeds in up to 95 % yield and with 100 % regioselectivity while the corresponding alcohols were observed as side products.

Ruthenium-catalyzed transfer hydrogenation of amino- and amido-substituted acetophenones

The ruthenium-catalyzed transfer hydrogenation of electron-rich amino-substituted acetophenones is reported. Variation of the reductant, ligands, base, and solvent allowed reaction optimization. A key discovery was the use of 1,4-butanediol as an irreversible reducing agent, which significantly improved the conversion. A range of amino- and amido-substituted aryl ketones were explored, and they all gave the corresponding alcohols in good yield, which demonstrates the wider applicability of this process. The ruthenium-catalyzed reduction of electron-rich amino-substituted acetophenones with 1,4-butanediol as an irreversible reducing agent is reported. Optimization of the conditions and variation of the amino substituent are explored as is the use of amido- and sulfonamidoacetophenones with varying results. Copyright