2-Chloro-6-methylphenol → 3-Chloro-4-hydroxy-5-methylbenzonitrile
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[OH:9].C(C1C=C(C=C(C)C=1O)[C:15]#[N:16])C>>[Cl:1][C:2]1[CH:7]=[C:6]([CH:5]=[C:4]([CH3:8])[C:3]=1[OH:9])[C:15]#[N:16]Participants
3
Procedure
The title compound is prepared from commercially available 2-chloro-6-methyl-phenol in analogy to literature procedures (see 3-ethyl-4-hydroxy-5-methyl-benzonitrile); LC-MS: tR=0.85 min. 1H NMR (CDCl3): δ2.33 (s, 3H), 6.10 (s, 1H), 7.38 (s, 1H), 7.53 (d, J=1.8 Hz, 1H).
Sources & evidence
- ORD record
- ord-63e0f18fff9c4b90a23fbc9e6fb1e709
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09133179B2
Reaction notes
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