[C:1]1(S(OCC#C)(=O)=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:14]1([OH:20])C=C[CH:17]=[CH:16][CH:15]=1.C1C(O)=CC=CC=1C>>[CH2:14]([O:20][C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)[CH2:15][C:16]#[CH:17]The procedure for Example 614 was used, substituting 3-butynyl p-toluenesulfonate for propargyl benzenesulfonate and phenol for m-cresol to provide Example 633. 1H NMR (500 MHz, CDCl3) δ 2.02 (t, J=2 Hz, 1H), 2.68 (dt, J=8, 2 Hz, 2H), 4.08 (t, J=8 Hz, 2H), 6.96 (m, 3H), 7.30 (m, 2H).
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