Iodoethane → HCID 86587906, compound
Reaction equation
[F:1][C:2]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:3]=1[C:4]#N.[CH2:11](I)[CH3:12].[C:14]([NH:18][OH:19])([CH3:17])([CH3:16])[CH3:15]>>[F:1][C:2]1[CH:9]=[C:8]([O:10][CH2:11][CH3:12])[CH:7]=[CH:6][C:3]=1[CH:4]=[N+:18]([C:14]([CH3:17])([CH3:16])[CH3:15])[O-:19]Participants
4
Procedure
The title compound was prepared according to the procedure described in Example 29 using 2-fluoro-4-hydroxybenzonitrile, ethyl iodide and N-tert-butylhydroxylamine. The title compound was isolated in 64.7% overall yield as slightly yellowish crystals, m.p. 82.5° C. (Rf =0.16 on a silica gel plate using hexanes/ethyl acetate, 4:1, v:v, as the eluant).
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-437eb58115644ac89f037e986a0d9a52
- Source dataset
- uspto-grants-2000_04
- Patent number
- US06046232
Reaction notes
Loading…