Ethyl Acetate → 5-Amino-4-fluoro-2-(1-methylcyclohexyl)phenyl methyl carbonate

HRID 1465152Notes

Reaction equation

HRID 1465152 reaction equation
[C:1](=[O:22])([O:20][CH3:21])[O:2][C:3]1[CH:8]=[C:7]([N+:9]([O-])=O)[C:6]([F:12])=[CH:5][C:4]=1[C:13]1([CH3:19])[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1.C([O-])=O.[NH4+].C(OCC)(=O)C>CO.[Pd]>[C:1](=[O:22])([O:20][CH3:21])[O:2][C:3]1[CH:8]=[C:7]([NH2:9])[C:6]([F:12])=[CH:5][C:4]=1[C:13]1([CH3:19])[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1

Participants

6

Procedure

To a solution of 4-fluoro-2-(1-methylcyclohexyl)-5-nitrophenyl methyl carbonate 24.1 g, 77.5 mmol) in 220 mL of CH3OH was added Pd/C 10%, 9.6 g, then ammonium formate (26.7 g, 445 mmol) was portion-wise added to the above reaction mixture at room temperature until starting material is consumed. The mixture was filtrated and the filtrate was evaporated under vacuum. The residue was purified by column chromatography on silica gel diluted with hexane:ethyl acetate=50:1 to give 5-amino-4-fluoro-2-(1-methylcyclohexyl)phenyl methyl carbonate as a red brown oil (17.9 g, 82% yield). 1H NMR (400 MHz, CDCl3) δ 6.99 (d, J=13.6 Hz, 1 H), 6.51 (d, J=8.4 Hz, 1H), 3.89 (s, 3 H), 3.43 (brs, 2H), 1.96-1.91 (m, 2H), 1.58-1.38 (m, 8H), 1.18 (s, 3H): MS m/z: 281.9 [M+H]+

Workup

  1. additionadded to the above reaction mixture at room temperature
  2. customis consumed
  3. filtrationThe mixture was filtrated
  4. customthe filtrate was evaporated under vacuum
  5. customThe residue was purified by column chromatography on silica gel
  6. additiondiluted with hexane

Sources & evidence

ORD record
ord-7658db72782c4ba3ad30b90f93e23a89
Source dataset
uspto-grants-2015_04
Patent number
US08999976B2

Reaction notes

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