Tetrahydro-4H-pyran-4-ol → HCID 66730461, compound
Reaction equation
[O:1]1[CH2:6][CH2:5][CH:4]([OH:7])[CH2:3][CH2:2]1.Br[CH2:9][CH2:10][CH2:11][O:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[CH2:13]([O:12][CH2:11][CH2:10][CH2:9][O:7][CH:4]1[CH2:5][CH2:6][O:1][CH2:2][CH2:3]1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1Participants
3
Procedure
Using tetrahydro-4-pyranol (0.693 mL, 7.27 mmol) and [(3-bromopropoxy)methyl]benzene (1.93 mL, 10.9 mmol), the desired title compound (437 mg, yield 24%) was obtained by the same method as in Reference Example 2 (2a).
Sources & evidence
- ORD record
- ord-87cd57c2c33e42f599bc6fbbacf53c03
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08410273B2
Reaction notes
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