Tetrabutylammonium Fluoride → 1-(4-Hydroxymethyl-1,3-thiazol-2-yl)-3-hydroxyazetidine
反応式
[Si]([O:18][CH:19]1[CH2:22][N:21]([C:23]2[S:24][CH:25]=[C:26]([CH2:28][OH:29])[N:27]=2)[CH2:20]1)(C(C)(C)C)(C1C=CC=CC=1)C1C=CC=CC=1.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1>[OH:29][CH2:28][C:26]1[N:27]=[C:23]([N:21]2[CH2:22][CH:19]([OH:18])[CH2:20]2)[S:24][CH:25]=1参加物
4
実験手順
To a solution of 3-t-butyldiphenylsilyloxy-1-(4-hydroxymethyl-1,3-thiazol-2-yl)azetidine (548.5 mg, 1.29 mmol) (obtained as described in Reference Example 2(2)) in anhydrous tetrahydrofuran (28 ml) was added a solution of 1.0M tetra-n-butylammonium fluoride in tetrahydrofuran (1.56 ml, 1.56 mmol) in an ice bath, and the mixture was then stirred in the ice bath for 1 hour. After checking the completion of the reaction, the reaction mixture was concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using ethyl acetate:methanol (10:1) as the eluant to afford 1-(4-hydroxymethyl-1,3-thiazol-2-yl)-3-hydroxyazetidine (230 mg, yield 96%) as a white solid.