Water → HCID 20521609, compound
Reaction equation
[C:1]([OH:9])#[C:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH2:10]([Li])[CH2:11][CH2:12][CH3:13].[CH3:15][S:16](Cl)(=[O:18])=[O:17].[OH2:20].C([O:23][CH2:24]C)C>CCCCCC>[O:23]1[CH2:24][CH2:13][CH2:12][CH2:11][CH:10]1[O:9][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][C:6]#[C:7][CH2:8][O:17][S:16]([CH3:15])(=[O:18])=[O:20]Participants
Reactant 5
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
Under an atmosphere of nitrogen, a solution of 4.2 g of the octyn-1-ol compound (prepared as described above) in 10 ml of diethyl ether was added dropwise to 12.8 ml of an 1.45 M solution of butyl lithium in hexane at 0° C., the mixture was stirred at 0° C. for 30 minutes. To the solution was added dropwise a solution of 1.58 ml of methanesulphonyl chloride in 7 ml of diethyl ether, then stirred at 0° C. for 3 hours. The mixture was poured into cold water, extracted with diethyl ether, the extract was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulphate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixture of ethyl acetate and hexane (3:7) as eluent to give 4.1 g of the subtitle compound having the following physical characteristics:
Workup
- stirringstirred at 0° C. for 3 hours
- extractionextracted with diethyl ether
- washthe extract was washed with a saturated aqueous solution of sodium chloride
- dry with materialdried over magnesium sulphate
- concentrationconcentrated under reduced pressure
- customThe residue was purified by column chromatography on silica gel using
- additiona mixture of ethyl acetate and hexane (3:7) as eluent
Sources & evidence
- ORD record
- ord-b6d86580a8bf47fda160c801d3ed37f9
- Source dataset
- uspto-grants-1982_10
- Patent number
- US04355170
Reaction notes
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