2-Bromoethanol → HCID 59971154, compound
Reaction equation
[CH3:1][O:2][CH2:3][C@@H:4]1[CH2:8][CH2:7][CH2:6][NH:5]1.Br[CH2:10][CH2:11][OH:12]>>[OH:12][CH2:11][CH2:10][N:5]1[CH2:6][CH2:7][CH2:8][C@H:4]1[CH2:3][O:2][CH3:1]Participants
3
Procedure
Using an analogous procedure to those described in Note [39] immediately above, (2S)-2-methoxymethylpyrrolidine was reacted with 2-bromoethanol to give (2S)-1-(2-hydroxyethyl)-2-methoxymethylpyrrolidine; NMR Spectrum: (CDCl3) 1.5–1.65 (m, 1H), 1.65–1.8 (m, 2H), 1.8–2.0 (m, 2H), 2.3 (m, 1H), 2.6 (m, 1H), 2.8 (m, 1H), 2.95–3.05 (m, 1H), 3.17 (m, 1H), 3.3 (t, 1H, 3.35 (t, 1H), 3.37 (s, 3H), 3.5–3.7 (m, 2H).
Sources & evidence
- ORD record
- ord-2faced8f3a9a4774bebc3e2c41e00320
- Source dataset
- uspto-grants-2006_05
- Patent number
- US07049438B2
Reaction notes
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