Hydrochloric Acid → 4-Bromo-2-{[(2R)-morpholin-2-yl]methyl}phenol
Reaction equation
C([N:8]1[CH2:13][CH2:12][O:11][C@H:10]([CH2:14][C:15]2[CH:20]=[C:19]([Br:21])[CH:18]=[CH:17][C:16]=2[OH:22])[CH2:9]1)(OC(C)(C)C)=O.Cl>>[Br:21][C:19]1[CH:18]=[CH:17][C:16]([OH:22])=[C:15]([CH:20]=1)[CH2:14][C@H:10]1[O:11][CH2:12][CH2:13][NH:8][CH2:9]1Participants
3
Procedure
Deprotection of N-Boc-(R)-2-(5-bromo-2-hydroxybenzyl)morpholine, using hydrogen chloride (4M, in methanol), afforded the morpholine example 1 as an off-white solid (51 mg, 100%).
Sources & evidence
- ORD record
- ord-afc4bd7fa5534e3686f9306bdd5ffc8d
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07323466B2
Reaction notes
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