Glyoxylic Acid → HCID 68047230, compound
Reaction equation
[F:1][C:2]([F:16])([F:15])[C:3]1[CH:4]=[CH:5][C:6]([O:13][CH3:14])=[C:7]([CH2:9][C:10](=[O:12])[CH3:11])[CH:8]=1.[C:17]([OH:21])(=[O:20])[CH:18]=O>>[OH:12][C:10]1([CH3:11])[O:21][C:17](=[O:20])[CH:18]=[C:9]1[C:7]1[CH:8]=[C:3]([C:2]([F:15])([F:16])[F:1])[CH:4]=[CH:5][C:6]=1[O:13][CH3:14]Participants
3
Conditions
- Temperature
- 100 °C
Procedure
5-(Trifluoromethyl)-2-methoxyphenylacetone (2800 mg, 12 mmol) was mixed with glyoxylic acid (2.7 mL 18 mmol) and stirred at 100° C. for 16 hours. The reaction mixture was then concentrated in vacuo and azeotroped with toluene to afford the title compound (3.5 g).
Workup
- concentrationThe reaction mixture was then concentrated in vacuo
- customazeotroped with toluene
Sources & evidence
- ORD record
- ord-d6ffa2db25ee49ce898092ab539e07f8
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09145407B2
Reaction notes
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