Oxalyl chloride → HCID 18999946, compound
Reaction equation
[CH3:1][CH:2]([CH3:10])[CH2:3][CH2:4][C:5](=[O:9])[C:6](O)=[O:7].C(Cl)(=O)C([Cl:14])=O>>[CH3:1][CH:2]([CH3:10])[CH2:3][CH2:4][C:5](=[O:9])[C:6]([Cl:14])=[O:7]Participants
3
Procedure
The 5-methyl-2-oxohexanoic acid is reacted with at least a 10% excess over the stoichiometric amount of oxalyl chloride to form 5-methyl-2-oxohexanoyl chloride [reaction (4)]. ##EQU6## Oxalyl chloride is a suitable solvent for reaction (4), and theoretically can be present in an unlimited excess over stoichiometry. Solvents such as diethyl ether, petroleum ether, benzene, CH2Cl2, and hexane are also suitable solvents for the reaction. The use of solvents is preferred but is not necessary. Reaction (4) must be run under anhydrous conditions in an inert atmosphere and requires from 40 to 60 hours at a temperature of from 25° to 60° C. for completion.
Sources & evidence
- ORD record
- ord-2077c4052ccb4e8f946c101dfdcd0840
- Source dataset
- uspto-grants-1976_05
- Patent number
- US03959312
Reaction notes
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