(4-Chloro-3-(trifluoromethoxy)phenyl)methanol → 4-Chloro-3-(trifluoromethoxy)benzyl bromide
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8]O)=[CH:4][C:3]=1[O:10][C:11]([F:14])([F:13])[F:12].[Br:15]C1C=C(CBr)C=CC=1OC(F)(F)F>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][Br:15])=[CH:4][C:3]=1[O:10][C:11]([F:14])([F:13])[F:12]Participants
3
Procedure
Compound 35.2 was synthesized from (4-chloro-3-(trifluoromethoxy)phenyl)-methanol using the procedure described for the preparation of 19.2. 1H NMR (500 MHz, DMSO-d6) δ 7.74 (1 H, d, J=2.0 Hz), 7.38-7.53 (2 H, m), 4.53 (2 H, d, J=5.6 Hz)
Sources & evidence
- ORD record
- ord-40c0225e8a9648c797f3a2da478fc80a
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08003648B2
Reaction notes
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