Methyl morpholine oxide → HCID 86597845, compound
Reaction equation
[CH2:1]([O:3][C:4]1[C:5](/[C:16](/[CH2:21][CH3:22])=[C:17](/[F:20])\[CH2:18][OH:19])=[CH:6][C:7]2[CH:8]=[CH:9][CH2:10][C:11]([CH3:15])([CH3:14])[C:12]=2[CH:13]=1)[CH3:2].C[N+]1([O-])CCOCC1>>[CH2:1]([O:3][C:4]1[C:5](/[C:16](/[CH2:21][CH3:22])=[C:17](/[F:20])\[CH:18]=[O:19])=[CH:6][C:7]2[CH:8]=[CH:9][CH2:10][C:11]([CH3:14])([CH3:15])[C:12]=2[CH:13]=1)[CH3:2]Participants
3
Procedure
Following General Procedure H-1, (2E)-3-(3-ethoxy-5,5-dimethyl-5,6-dihydro-naphthalen-2-yl)-2-fluoro-pent-2-en-1-ol (Compound A-50, 35 mg, 0.12 mmol) and 4-methylmorpholine N-oxide (27 mg, 0.23 nmol) were reacted to give the title compound as a yellow solid after purification by flash chromatography (silica gel, 10% ethyl acetate in hexanes).
Workup
- customwere reacted
Sources & evidence
- ORD record
- ord-f73cde027d424cce80f67ad1455a18cd
- Source dataset
- uspto-grants-2005_05
- Patent number
- US06887896B1
Reaction notes
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