Water → 4-Chloroquinoline-6-carbaldehyde

HRID 1952315Notes

Reaction equation

HRID 1952315 reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([CH:12]=C)[CH:10]=2)[N:5]=[CH:4][CH:3]=1.N1C(C)=CC=CC=1C.[O-:22]I(=O)(=O)=O.[Na+].O>C(O)(C)(C)C.O1CCOCC1.[Os](=O)(=O)(=O)=O>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([CH:12]=[O:22])[CH:10]=2)[N:5]=[CH:4][CH:3]=1

Participants

8

Reactant 4

HCID 962WaterHCID 79372,6-LutidineHCID 23667635Sodium periodateHCID 59822492HCID 59822492, compound

Product 1

HCID 534172264-Chloroquinoline-6-carbaldehydeYield 83%

Reagents, catalysts & solvents 3

HCID 30318Osmium TetroxideCatalystHCID 6386tert-ButanolSolventHCID 312751,4-DioxaneSolvent

Procedure

A mixture of 4-chloro-6-ethenylquinoline (5.1 g, 26.88 mmol), 2,6-lutidine (5.76 g, 53.75 mmol), sodium (meta) periodate (22.99 g, 107.51 mmol), and osmium tetroxide (5.48 g of a 2.5% solution in tert-butanol, 0.538 mmol) in 1,4-dioxane:H2O (350 mL of 3:1 mixture) was stirred for 3.5 h at room temperature and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (CH2Cl2) to give the title compound (4.26 g, 83% for 2 steps) as a pale yellow solid. MS (ES)+ m/e 192 [M+H]+.

Workup

  1. concentrationconcentrated in vacuo
  2. customThe residue was purified by flash chromatography on silica gel (CH2Cl2)

Sources & evidence

ORD record
ord-dffb63f007474f9ea9883fa4006cd0a7
Source dataset
uspto-grants-2013_03
Patent number
US08404837B2

Reaction notes

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