1,5-Hexadiene → HCID 87608833, compound
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
Reactant 3
Product 1
Reagents, catalysts & solvents 1
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
- customquenched with water
- extractionThe mixture was extracted with diethyl ether
- washthe diethyl ether layer was washed with saturated sodium bicarbonate solution
- dry with materialdried with sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-c80beab960f442068c9f9996d8ce1711
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07378414B2
Reaction notes
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