Basic information
- CAS
2258-42-6- Standard SMILES
CC(=O)OC=O- InChIKey
ORWKVZNEPHTCQE-UHFFFAOYSA-N- Molecular formula
- C3H4O3
- Average molar mass
- 88.06 g/mol
- Monoisotopic mass
- 88.01604399
Names & identifiers
- Preferred name
- Acetic-formic anhydride
- IUPAC
- formyl acetate
- English name
- Formyl acetate
- Molecular formula
- C3H4O3
- Molecular weight
- 88.06
Names & synonyms
Show more names
Database identifiers
- CAS
2258-42-6- PubChem CID
- 75269
- DTXSID
DTXSID80177103- UNII
- GNF4F3WBU5
- Nikkaji
- J24.126A
Properties
Computed structural properties
- XLogP
- -0.1
- Topological polar surface area
- 43.4 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 3
- Rotatable bonds
- 2
- Heavy atoms
- 6
- Formal charge
- 0
- Complexity
- 66.4
Experimental & physicochemical properties
Physicochemical properties
- Boiling point
- 27 · 27-28 °C(Press: 1 Torr)
- Density
- 1.116 · 1.116±0.06 g/cm3(Predicted)
- solubility
- Chloroform (Slightly), Ethyl Acetate (Soluble), Methanol (Slightly)
- form
- Oil
- color
- Colourless
- Stability
- Air Sensitive, Hygroscopic
- FDA UNII
- 4 F3WBU5 · GNF4F3WBU5
- HS Code
- 29159000 · 29159000
Safety & regulation
Safety data
- hs_code
- 29159000
Chemistry & industry
Applications
DescriptionAcetic formic anhydride, or ethanoic methanoic anhydride is a chemical compound with formula C3H4O3, or H3C-(C=O)-O-(C=O)H. It can be viewed as the mixed anhydride of acetic acid (H3C- (C=O)OH) and formic acid (H(C= O)OH) by removal of a molecule of water. It can be produced by reaction between sodium formate and acetyl chloride in anhydrous diethyl ether, at 23–27 °C.Among other uses, it is a formylation agent for amines, amino acids, and alcohols, and a starting material for formyl fluoride.
UsesFormyl acetate is a useful formylating agent for the hydroxyl, phenol, and amine groups as well as other heteroatoms; useful for the synthesis of aldehydes from aromatic Grignard reagents, for the preparation of formyl fluoride, and for the preparation of diazoacetaldehyde.
Preparation methods
PreparationPreparative Methods of Formyl acetate: acetic formic anhydride is not comercially available. The easiest method of preparation is by the reaction of sodium formate and Acetyl Chloride in dry ether as reported by Krimen. Alternatively, Ketene and Formic Acid form the title compound at room temperature or below. Acetic formic anhydride can be prepared rapidly in situ by stirring formic acid, acetyl chloride, and Triethylamine in THF at -70 °C for 10 min. AFA is found in a mixture of formic acid (excess) with Acetic Anhydride. The mixture is more accurately described as formic acid-acetic anhydride mixture (FAM) and is also used as a formylating agent. Purification: by fractional distillation at low pressure.
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers43 total
Related reactions
Compound notes
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