Acetyl chloride → HCID 10797860, compound
Reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[C:4]([CH3:9])[C:3]=1[OH:10].C([N:13](CC)CC)C.[C:18](Cl)(=[O:20])[CH3:19]>C(OCC)(=O)C>[C:18]([O:10][C:3]1[C:4]([CH3:9])=[C:5]([C:6]([CH3:8])=[CH:7][C:2]=1[CH3:1])[NH2:13])(=[O:20])[CH3:19]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 2,4,6-trimethylphenol (10 g, 73.5 mmol) and triethylamine (11.1 g, 110.3 mmol) in ethyl acetate (200 mL) was added acetyl chloride (7.5 g, 95.6 mmol) dropwise at 0° C. The mixture was stirred overnight. The reaction was quenched with water and the organic layer was washed with 1 N HCl. The organic layer was dried and concentrated as usual. The residue was nitrated Example 14 (procedure B) and reduced as demonstrated for Example 14 (procedure C) to give 3-acetoxy-2,4,6-trimethylaniline.
Workup
- customThe reaction was quenched with water
- washthe organic layer was washed with 1 N HCl
- customThe organic layer was dried
- concentrationconcentrated as usual
Sources & evidence
- ORD record
- ord-9cd3ec0002404244a3d3b68dcc05f590
- Source dataset
- uspto-grants-2002_07
- Patent number
- US06420567B1
Reaction notes
Loading…