Hydrochloric Acid → 74975-02-3
Reaction equation
[CH3:1][C:2]1([CH3:12])[CH2:7][CH:6](/[CH:8]=[CH:9]/[O:10]C)[CH2:5][CH2:4][O:3]1.Cl>C1COCC1>[CH3:1][C:2]1([CH3:12])[CH2:7][CH:6]([CH2:8][CH:9]=[O:10])[CH2:5][CH2:4][O:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 20 °C
Procedure
To a stirred solution of 2,2-dimethyl-4-[(E)-2-(methyloxy)ethenyl]tetrahydro-2H-pyran (2.93 g, 17.21 mmol) in THF (15 ml) was added 2N HCl (15 ml, 30.0 mmol) and the mixture was stirred at 20° C. After 1 hour the mixture was extracted with diethyl ether (3×25 ml); the combined ether extracts dried (Na2SO4), filtered and evaporated in vacuo (at 50 mbar and water bath at 15° C.) to give the title compound as a pale yellow oil (2.56 g).
Workup
- extractionAfter 1 hour the mixture was extracted with diethyl ether (3×25 ml)
- dry with materialthe combined ether extracts dried (Na2SO4)
- filtrationfiltered
- customevaporated in vacuo (at 50 mbar and water bath at 15° C.)
Sources & evidence
- ORD record
- ord-0db80cf53d7649618c8257dd5e7a6e9a
- Source dataset
- uspto-grants-2011_07
- Patent number
- US07977344B2
Reaction notes
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