Methanol → 2,4,5-Trifluoro-6-methoxyisophthalonitrile
Reaction equation
[F:1][C:2]1[C:7]([C:8]#[N:9])=[C:6]([F:10])[C:5]([C:11]#[N:12])=[C:4](F)[C:3]=1[F:14].[CH3:15][OH:16]>>[F:10][C:6]1[C:7]([C:8]#[N:9])=[C:2]([F:1])[C:3]([F:14])=[C:4]([O:16][CH3:15])[C:5]=1[C:11]#[N:12]Participants
3
Procedure
A 2.0 g amount of tetrafluoroisophthalonitrile was heated under reflux in 40 ml of methanol for 4 hours. The methanol was distilled off in vacuo to approximately one-fifth volume and ice water was then poured to the resultant mixture. The precipitated crystal was collected by filtration and was then washed with water and a small amount of cold methanol. After drying in vacuo, 1.6 g of the desired compound No. 20 was obtained.
Workup
- distillationThe methanol was distilled off in vacuo to approximately one-fifth volume and ice water
- additionwas then poured to the resultant mixture
- filtrationThe precipitated crystal was collected by filtration
- washwas then washed with water
- dry with materialAfter drying in vacuo, 1.6 g of the desired compound No
- custom20 was obtained
Sources & evidence
- ORD record
- ord-d98562553b3f49f6b58c599eed5929bd
- Source dataset
- uspto-grants-1986_09
- Patent number
- US04614742
Reaction notes
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