1,4-Dioxane hydrochloride → 76391-36-1
Reaction equation
C(OC([N:8]1[CH2:12][C@H:11]([O:13][CH3:14])[CH2:10][C@H:9]1[C:15]([O:17][CH3:18])=[O:16])=O)(C)(C)C.[ClH:19].O1CCOCC1>>[ClH:19].[CH3:14][O:13][C@H:11]1[CH2:12][NH:8][C@H:9]([C:15]([O:17][CH3:18])=[O:16])[CH2:10]1Participants
3
Procedure
A solution of (2S,4R)-1-tertbutoxycarbonyl-2-methoxycarbonyl-4-methoxy pyrrolidine (9 g, 34.74 mmol) in 4 M HCl-dioxane (13 mL) was stirred at RT overnight. The reaction mixture was concentrated to dryness, washed with hexane followed by ether and dried under vacuum to afford (2S,4R)-methyl 4-methoxypyrrolidine-2-carboxylate hydrochloride (6 g).
Workup
- concentrationThe reaction mixture was concentrated to dryness
- washwashed with hexane
- customdried under vacuum
Sources & evidence
- ORD record
- ord-f62894f887324844a0d324f6b7b5f287
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09422267B2
Reaction notes
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