Hydrochloric Acid → HCID 14784508, compound
Reaction equation
C([Li])CCC.[C:6]1([CH2:12][C:13]([OH:15])=[O:14])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.Br[CH2:17][CH2:18][Cl:19].Cl>CCCCCC.C1COCC1.C(OCC)(=O)C>[Cl:19][CH2:18][CH2:17][CH:12]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[C:13]([OH:15])=[O:14]Participants
Conditions
- Temperature
- -78 °C
Procedure
A 2.64 M solution of butyl lithium in hexane (28 mL) was added to a solution of phenylacetic acid (5.07 g) in THF (150 mL) in a nitrogen atmosphere at −78° C., and the reaction solution was stirred at −78° C. for 20 minutes. The reaction solution was further stirred at 0° C. for one hour. Then, 1-bromo-2-chloroethane (3.1 mL) was added at 0° C., and the reaction solution was stirred at room temperature for 14 hours. Ethyl acetate and 1 N hydrochloric acid were added to the reaction solution, and the organic layer was separated. The resulting organic layer was washed with a saturated sodium chloride solution. The resulting organic layer was dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: heptane-ethyl acetate system) to obtain 5.54 g of the title compound. The property values of the compound are as follows.
Workup
- stirringThe reaction solution was further stirred at 0° C. for one hour
- stirringthe reaction solution was stirred at room temperature for 14 hours
- customthe organic layer was separated
- washThe resulting organic layer was washed with a saturated sodium chloride solution
- dry with materialThe resulting organic layer was dried over magnesium sulfate
- concentrationconcentrated under reduced pressure
- customThe residue was purified by silica gel column chromatography (elution solvent: heptane-ethyl acetate system)
Sources & evidence
- ORD record
- ord-09db7fb5bde545b29894f77538484579
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07935815B2
Reaction notes
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