1,5-Hexadiene → HCID 87608833, compound

HRID 494535Notes

Reaction equation

HRID 494535 reaction equation
[CH3:1][C:2]([CH3:9])([CH3:8])[CH2:3][CH:4](O)[CH:5]=[CH2:6].C=CCCC=C.S(Br)([Br:18])=O>ClCCCl>[Br:18][CH2:6]/[CH:5]=[CH:4]/[CH2:3][C:2]([CH3:9])([CH3:8])[CH3:1]

Participants

5

Conditions

Temperature
0 °C

Procedure

To a solution of Example 35A (2.38 g, 18.56 mmol) and 1,5-hexadiene (1.65 mL, 13.9 mmol) in 1,2-dichloroethane (30 mL),stirring at 0° C., was added thionyl bromide (2.16 mL, 27.8 mmol). The reaction was stirred for 2 hours at 0° C. and then quenched with water. The mixture was extracted with diethyl ether and the diethyl ether layer was washed with saturated sodium bicarbonate solution, dried with sodium sulfate, filtered, and concentrated in vacuo to give the title compound 3.15 g, 89%). 1H NMR (300 MHz, CDCl3): δ ppm 0.87 (m, 9 H) 1.94 (m, 2 H) 3.97 (m, 2 H) 5.74 (m, 2 H).

Workup

  1. customquenched with water
  2. extractionThe mixture was extracted with diethyl ether
  3. washthe diethyl ether layer was washed with saturated sodium bicarbonate solution
  4. dry with materialdried with sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-65ec891afd4e4db8809ac81b0021cd62
Source dataset
uspto-grants-2009_05
Patent number
US07538105B2

Reaction notes

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