We are working to restore the Unionpedia app on the Google Play Store
OutgoingIncoming
🌟We've simplified our design for better navigation!
Instagram Facebook X LinkedIn

Casiraghi formylation

Index Casiraghi formylation

In organic synthesis, the Casiraghi formylation is the formation of a salicylaldehyde from a phenol and paraformaldehyde. [1]

Table of Contents

  1. 13 relations: Brønsted–Lowry acid–base theory, Cannizzaro reaction, Derivative (chemistry), Directed ortho metalation, Friedel–Crafts reaction, Grignard reagent, Lewis acids and bases, Methanol, Organic synthesis, Paraformaldehyde, Phenol, Salicylaldehyde, Tocopherol.

  2. Benzaldehydes

Brønsted–Lowry acid–base theory

The Brønsted–Lowry theory (also called proton theory of acids and bases) is an acid–base reaction theory which was first developed by Johannes Nicolaus Brønsted and Thomas Martin Lowry independently in 1923.

See Casiraghi formylation and Brønsted–Lowry acid–base theory

Cannizzaro reaction

The Cannizzaro reaction, named after its discoverer Stanislao Cannizzaro, is a chemical reaction which involves the base-induced disproportionation of two molecules of a non-enolizable aldehyde to give a primary alcohol and a carboxylic acid.

See Casiraghi formylation and Cannizzaro reaction

Derivative (chemistry)

In chemistry, a derivative is a compound that is derived from a similar compound by a chemical reaction.

See Casiraghi formylation and Derivative (chemistry)

Directed ortho metalation

Directed ortho metalation (DoM) is an adaptation of electrophilic aromatic substitution in which electrophiles attach themselves exclusively to the ortho- position of a direct metalation group or DMG through the intermediary of an aryllithium compound.

See Casiraghi formylation and Directed ortho metalation

Friedel–Crafts reaction

The Friedel–Crafts reactions are a set of reactions developed by Charles Friedel and James Crafts in 1877 to attach substituents to an aromatic ring.

See Casiraghi formylation and Friedel–Crafts reaction

Grignard reagent

Grignard reagents or Grignard compounds are chemical compounds with the general formula, where X is a halogen and R is an organic group, normally an alkyl or aryl.

See Casiraghi formylation and Grignard reagent

Lewis acids and bases

A Lewis acid (named for the American physical chemist Gilbert N. Lewis) is a chemical species that contains an empty orbital which is capable of accepting an electron pair from a Lewis base to form a Lewis adduct.

See Casiraghi formylation and Lewis acids and bases

Methanol

Methanol (also called methyl alcohol and wood spirit, amongst other names) is an organic chemical compound and the simplest aliphatic alcohol, with the chemical formula (a methyl group linked to a hydroxyl group, often abbreviated as MeOH).

See Casiraghi formylation and Methanol

Organic synthesis

Organic synthesis is a branch of chemical synthesis concerned with the construction of organic compounds.

See Casiraghi formylation and Organic synthesis

Paraformaldehyde

Paraformaldehyde (PFA) is the smallest polyoxymethylene, the polymerization product of formaldehyde with a typical degree of polymerization of 8–100 units.

See Casiraghi formylation and Paraformaldehyde

Phenol

Phenol (also known as carbolic acid, phenolic acid, or benzenol) is an aromatic organic compound with the molecular formula.

See Casiraghi formylation and Phenol

Salicylaldehyde

Salicylic aldehyde (2-hydroxybenzaldehyde) is an organic compound with the formula.

See Casiraghi formylation and Salicylaldehyde

Tocopherol

Tocopherols (TCP) are a class of organic compounds comprising various methylated phenols, many of which have vitamin E activity.

See Casiraghi formylation and Tocopherol

See also

Benzaldehydes

References

[1] https://en.wikipedia.org/wiki/Casiraghi_formylation