M-Cresol → Tert-butyl 3-(m-tolyloxy)pyrrolidine-1-carboxylate
Reaction equation
[C:1]([N:8]1[CH2:12][CH2:11][CH:10]([OH:13])[CH2:9]1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[CH3:14][C:15]1[CH:16]=[C:17](O)[CH:18]=[CH:19][CH:20]=1>>[C:15]1([CH3:14])[CH:16]=[CH:17][CH:18]=[C:19]([O:13][CH:10]2[CH2:11][CH2:12][N:8]([C:1]([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2])[CH2:9]2)[CH:20]=1Participants
3
Procedure
The title compound (D38) (1.59 g) was prepared according to the experimental procedure described in Description 34 starting from 1-Boc-3-pyrrolidinol (1 g, 5.34 mmol) and 3-Methylphenol (0.558 ml, 5.34 mmol).
Sources & evidence
- ORD record
- ord-1636a5ec1d944ed6b40c48acc062b179
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08828987B2
Reaction notes
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