Glycolic Acid → HCID 4066944, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([NH2:10])[C:5]([NH:8][CH3:9])=[CH:6][CH:7]=1.[C:11]([OH:15])(=O)[CH2:12]O>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]2[N:8]([CH3:9])[C:12]([CH2:11][OH:15])=[N:10][C:4]=2[CH:3]=1Participants
3
Conditions
- Temperature
- 150 °C
Procedure
4-chloro-N1-methylbenzene-1,2-diamine (15.0 g, 96 mmol) and glycolic acid (8.1 g, 106 mmol) were mixed together in a sealed tube. The mixture was heated at 150° C. for 5 hours before it was cooled down to room temperature. The residue was purified by flash column chromatography (0–5% MeOH in CH2Cl2) to give the product (8.5 g, 45% yield). 1H NMR (300 MHz, CDCl3) δ: 3.80 (s, 3 H), 4.86 (s, 2 H), 7.13–7.22 (m, 2 H), 7.62–7.64 (m, 1 H).
Workup
- temperaturewas cooled down to room temperature
- customThe residue was purified by flash column chromatography (0–5% MeOH in CH2Cl2)
Sources & evidence
- ORD record
- ord-191ec4c30898423e848e4edca8d36c9e
- Source dataset
- uspto-grants-2006_12
- Patent number
- US07148226B2
Reaction notes
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