Benzoyl chloride, 3-chloro- → HCID 58573538, compound

HRID 1048253Notes

Reaction equation

HRID 1048253 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5](Cl)=[O:6].[CH2:11]([Mg]Br)[CH2:12][CH:13]=[CH2:14]>C1COCC1.[Cu]I>[Cl:1][C:2]1[CH:3]=[C:4]([C:5](=[O:6])[CH2:14][CH2:13][CH:12]=[CH2:11])[CH:8]=[CH:9][CH:10]=1

Participants

5

Conditions

Temperature
-10 °C

Procedure

To a solution of 3-chlorobenzoyl chloride (7 ml, 54.7 mmol) in THF (60 mL) was added copper (I) iodide (0.521 g, 2.73 mmol). The slurry was cooled to −10° C. and 3-butenylmagnesium bromide (0.5M in THF) (112 ml, 55.8 mmol) was added dropwise via cannula over 30 min. The reaction mixture was stirred at −10° C. for 1 h and then warmed to room temperature. The reaction mixture was concentrated to 25 mL and diluted with 100 mL DCM and 100 mL 1M HCl. The layers were separated and the organic layer was filtered. The filtrate was washed with sat. NaHCO3, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (eluent: 0 to 50% DCM in hexanes) to give the title compound.

Workup

  1. temperaturewarmed to room temperature
  2. concentrationThe reaction mixture was concentrated to 25 mL
  3. additiondiluted with 100 mL DCM and 100 mL 1M HCl
  4. customThe layers were separated
  5. filtrationthe organic layer was filtered
  6. washThe filtrate was washed with sat. NaHCO3
  7. dry with materialdried over Na2SO4
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by flash chromatography on silica gel (eluent: 0 to 50% DCM in hexanes)

Sources & evidence

ORD record
ord-c47b5e2ceb264a49a3a104323231c689
Source dataset
uspto-grants-2013_10
Patent number
US08569341B2

Reaction notes

Loading…