2-(3-Ethoxy-5-ethyl-2-fluorophenyl)-2-hydroxyacetonitrile → 2-(5-Ethyl-2-fluoro-3-methoxyphenyl)-2-hydroxyacetonitrile
Reaction equation
C(C1C=C(OC)C(F)=C(C=1)C=O)C.[CH2:14]([O:16][C:17]1[C:18]([F:29])=[C:19]([CH:25]([OH:28])[C:26]#[N:27])[CH:20]=[C:21]([CH2:23][CH3:24])[CH:22]=1)C>>[CH2:23]([C:21]1[CH:22]=[C:17]([O:16][CH3:14])[C:18]([F:29])=[C:19]([CH:25]([OH:28])[C:26]#[N:27])[CH:20]=1)[CH3:24]Participants
3
Procedure
119B was prepared from 119A using a procedure similar to that used in the preparation of 118E. 1H NMR (400 MHz, CDCl3) δ ppm 1.23 (t, J=7.47 Hz, 3H) 2.64 (q, J=7.62 Hz, 2H) 3.89 (s, 3H) 5.76 (s, 1H) 6.86 (dd, J=7.91, 2.20 Hz, 1H) 6.98 (dd, J=5.93, 1.98 Hz, 1H).
Sources & evidence
- ORD record
- ord-99bd70eb62ba42deaace1ff199e1c0b3
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07622585B2
Reaction notes
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