Hydrochloric Acid → HCID 70277877, compound
Reaction equation
C(OC([N:8]1[CH2:12][C@H:11]([O:13][Si](C(C)(C)C)(C)C)[CH2:10][C@H:9]1[C:21](=[O:32])[CH2:22][CH2:23][O:24][Si](C(C)(C)C)(C)C)=O)(C)(C)C.CO.[ClH:35]>>[ClH:35].[OH:13][C@H:11]1[CH2:12][NH:8][C@H:9]([C:21](=[O:32])[CH2:22][CH2:23][OH:24])[CH2:10]1Participants
4
Procedure
(2S,4R)-N-tert-Butoxycarbonyl-4-tert-butyldimethylsiloxy-2-(3-tert-butyldimethylsiloxy-1-oxopropyl)pyrrolidine (4.87 g, 10.0 mmol) was dissolved in a 3.3N hydrogen chloride--methanol solution (16.5 ml). The solution was stirred at room temperature for 24 h, and then concentrated in vacuo to obtain the title compound (2.29 g).
Workup
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-68f60f7885c845d7b9a48238786ac111
- Source dataset
- uspto-grants-1996_08
- Patent number
- US05550121
Reaction notes
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