4-Methylthiazole → 1-(2-Furyl)-1-(4-methyl-5-thiazolyl)ethanol
Reaction equation
[CH3:1][C:2]1[N:3]=[CH:4][S:5][CH:6]=1.[C:7]([C:10]1[O:11][CH:12]=[CH:13][CH:14]=1)(=[O:9])[CH3:8]>>[O:11]1[CH:12]=[CH:13][CH:14]=[C:10]1[C:7]([C:6]1[S:5][CH:4]=[N:3][C:2]=1[CH3:1])([OH:9])[CH3:8]Participants
3
Procedure
Starting with 4-methylthiazole and 2-acetylfuran and following the general method of Example 15 the title compound was prepared. M.p. 127°-128° C.
Sources & evidence
- ORD record
- ord-a210beaddfb84e2bacb0459a8fb6e751
- Source dataset
- uspto-grants-1998_03
- Patent number
- US05731335
Reaction notes
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