Ethyl Spiro[2.5]octane-1-carboxylate → 680619-21-0
Reaction equation
[CH:1]1([C:10]([O:12]CC)=[O:11])[C:3]2([CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]2)[CH2:2]1.C1(C(OCC)=O)C2(CCCCC2)C1>>[CH:1]1([C:10]([OH:12])=[O:11])[C:3]2([CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]2)[CH2:2]1Participants
3
Procedure
The title compound was prepared as described in Example 1B substituting the product from Example 39B for the product from Example 1A. 13C NMR (CDCl3, 100 MHz) δ 23.7, 26.2, 26.4, 27.2, 27.9, 28.0, 28.4, 31.2, 33.4, 33.5, 40.1, 179.3; MS m/z 168 (M)+.
Sources & evidence
- ORD record
- ord-175cbcaaa1094fcb829e797b12168998
- Source dataset
- uspto-grants-2011_04
- Patent number
- US07932245B2
Reaction notes
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