HNO3/Silica Gel supported CAN; Oxidative Deprotection of Benzylic Tetrahydropyranyl Ethers under Solvent-free Conditions using Microwaves

2005 ◽  
Vol 2005 (2) ◽  
pp. 105-106 ◽  
Author(s):  
Majid M. Heravi ◽  
Pegah Kazemian ◽  
Hossein A. Oskooie ◽  
Mitra Ghassemzadeh
Keyword(s):  
Ammonium Nitrate ◽  
Silica Gel ◽  
Carbonyl Compounds ◽  
Solvent Free ◽  
Cerium Ammonium Nitrate ◽  
Solvent Free Conditions ◽  
Cerium Ammonium

Benzylic tetrahydropyranyl ethers are rapidly and selectively oxidised to the corresponding carbonyl compounds by HNO3/ silica gel supported cerium ammonium nitrate (CAN) under solvent free conditions using microwave.

Efficient thioacetalisation of carbonyl compounds

2014 ◽  
Vol 68 (3) ◽  
Author(s):  
Davood Habibi ◽  
Payam Rahmani ◽  
Ziba Akbaripanah
Keyword(s):  
Reaction Time ◽  
Heterogeneous Catalyst ◽  
Sulphuric Acid ◽  
Silica Gel ◽  
Carbonyl Compounds ◽  
Solvent Free ◽  
Short Reaction Time ◽  
Solvent Free Conditions ◽  
Derivatives Of ◽  
Efficient Heterogeneous Catalyst

AbstractThe thioacetalisation of a variety of heterocyclic, aromatic, and aliphatic carbonyl compounds (1 mmol) with ethane-1,2-dithiol (1 mmol) using silica sulphuric acid (SSA) is presented as an efficient heterogeneous catalyst under mild and solvent-free conditions at 60°C. The thioacetals were formed within a short reaction time (1–34 min) and isolated with 90–98 % yield following an extractive procedure and chromatography on silica gel. The competitive protection reaction between aldehyde and ketone with ethane-1,2-dithiol afforded the protected derivatives of benzaldehyde and acetophenone with 92 % and 8 % yields, respectively, indicating some selectivity.

Regeneration of Carbonyl Compounds from Oximes and Hydrazones Using Peroxymonosulfate on Silica gel under Solvent-free Conditions

2000 ◽  
Vol 30 (17) ◽  
pp. 3121-3125 ◽  
Author(s):  
D. Subhas Bose ◽  
A. Venkat Narsaiah ◽  
V. Lakshminarayana
Keyword(s):  
Silica Gel ◽  
Carbonyl Compounds ◽  
Solvent Free ◽  
Solvent Free Conditions

Silica Gel Supported Sodium Hydrogen Sulfate as an Efficient and Reusable Heterogeneous Catalyst for the Synthesis of Imines in Solvent-free Conditions under Microwave Irradiation

2005 ◽  
Vol 2005 (5) ◽  
pp. 299-303 ◽  
Author(s):  
Mannathusamy Gopalakrishnan ◽  
Purushothaman Sureshkumar ◽  
Vijayakumar Kanagarajan ◽  
Jeyaraman Thanusu ◽  
Ramalingam Govindaraju
Keyword(s):  
Microwave Irradiation ◽  
Heterogeneous Catalyst ◽  
Silica Gel ◽  
Diethyl Ether ◽  
Carbonyl Compounds ◽  
Solvent Free ◽  
Hydrogen Sulfate ◽  
Sodium Hydrogen ◽  
Solvent Free Conditions

This synthesis of imines has been carried out efficiently by the condensation of carbonyl compounds with amines in the presence of silica gel supported sodium hydrogen sulfate (NaHSO4.SiO2) as a heterogeneous catalyst under microwave irradiation in solvent-free conditions. NaHSO4.SiO2 can be recovered and re-used up to ten times by simple washing with diethyl ether after each use and activated in an oven at 120 °C for 1 h, thus rendering the process more economical.

One-Pot, Regioselective Synthesis of Homopropargyl Alcohols using Propargyl Bromide and Carbonyl Compound by the Mg-mediated Reaction under Solvent-free Conditions

2020 ◽  
Vol 17 (6) ◽  
pp. 438-442
Author(s):  
Xiaofang Ma ◽  
Shunxi Li ◽  
Samrat Devaramani ◽  
Guohu Zhao ◽  
Daqian Xu
Keyword(s):  
Reaction Time ◽  
Organic Synthesis ◽  
Carbonyl Compounds ◽  
Solvent Free ◽  
Propargyl Bromide ◽  
Important Goal ◽  
One Pot ◽  
Short Reaction Time ◽  
Solvent Free Conditions ◽  
Volatile Organic

The elimination of volatile organic solvents in organic synthesis is the most important goal in “Green” chemistry. We report a simple, efficient and facile method for the addition of progargyl bromide to carbonyl compounds using Mg metal as a mediator under solvent-free conditions which could regioselectively generate homopropargyl alcohols efficiently in good to excellent yields. The procedure has advantages such as short reaction time, operationally simple, excellent product yields, high regioselectivity and organic solvent-free.

scholarly journals Tandem Fries Reaction–Conjugate Addition under Microwave Irradiation in Dry Media; One-pot Synthesis of Flavanones

1999 ◽  
Vol 23 (9) ◽  
pp. 574-575
Author(s):  
Firouz Matloubi Moghaddam ◽  
Mohammad Ghaffarzadeh ◽  
Seyed Hossein Abdi-Oskoui
Keyword(s):  
Microwave Irradiation ◽  
Silica Gel ◽  
Conjugate Addition ◽  
Solvent Free ◽  
Naphthalene Derivatives ◽  
One Pot ◽  
Fries Rearrangement ◽  
One Pot Synthesis ◽  
Solvent Free Conditions ◽  
Fries Reaction

An AICl3–ZnCl2 mixture supported on silica gel is found to be an efficient medium for the Fries rearrangement of acyloxybenzene or naphthalene derivatives in solvent-free conditions under microwave irradiation.

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