3-(Trifluoromethyl)phenol → 3-[3-(Trifluoromethyl)phenoxy]azetidine
Reaction equation
C([N:8]1[CH2:11][CH:10]([OH:12])[CH2:9]1)(OC(C)(C)C)=O.[F:13][C:14]([F:23])([F:22])[C:15]1[CH:16]=[C:17](O)[CH:18]=[CH:19][CH:20]=1>>[F:13][C:14]([F:23])([F:22])[C:15]1[CH:20]=[C:19]([CH:18]=[CH:17][CH:16]=1)[O:12][CH:10]1[CH2:9][NH:8][CH2:11]1Participants
3
Procedure
The title compound (D53) (100 mg) was prepared according to the experimental procedure described in Description 52 starting from 1-Boc-3-hydroxyazetidine (1 g, 5.77 mmol) and 3-(Trifluoromethyl)phenol (0.69 ml, 5.77 mmol).
Sources & evidence
- ORD record
- ord-4c56f6efe6d34c7cb22aed7d2cf12c39
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08828987B2
Reaction notes
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