Trifluoroacetic acid → 4-Methoxy-2-(trifluoromethyl)benzo[d]thiazole
Reaction equation
N[C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH3:12])[C:5]=2[N:6]=1.[F:13][C:14]([F:19])([F:18])C(O)=O>ClC1C=CC=CC=1Cl>[CH3:12][O:11][C:7]1[C:5]2[N:6]=[C:2]([C:14]([F:19])([F:18])[F:13])[S:3][C:4]=2[CH:10]=[CH:9][CH:8]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Starting from 2-amino-4-methoxybenzothiazole (1.5 g) and trifluoroacetic acid (5.5 ml), without 1,2 dichlorobenzene. Purification by flash chromatography (eluent 20% ethyl acetate/hexane) yielded the title compound as a light brown oil (0.74 g). TLC Rf 0.70 (50% ethyl acetate in hexane)
Workup
- customPurification by flash chromatography (eluent 20% ethyl acetate/hexane)
Sources & evidence
- ORD record
- ord-56ce66e72e984e86a4c202acdde71ffd
- Source dataset
- uspto-grants-2001_11
- Patent number
- US06313116B1
Reaction notes
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