Hydrochloric Acid → 869976-51-2
Reaction equation
[C:1]([C:5]1([OH:17])[CH2:9][CH2:8][N:7](C(OC(C)(C)C)=O)[CH2:6]1)([CH3:4])([CH3:3])[CH3:2].O1CCOCC1.[ClH:24]>>[ClH:24].[C:1]([C:5]1([OH:17])[CH2:9][CH2:8][NH:7][CH2:6]1)([CH3:4])([CH3:3])[CH3:2]Participants
4
Procedure
tert-Butyl 3-tert-butyl-3-hydroxypyrrolidine-1-carboxylate (0.60 g, 0.0025 mol) was dissolved in a solution of hydrogen chloride in 1,4-dioxane (4N, 0.30 mL, 0.0099 mol) under N2 at rt. The reaction mixture was stirred for 3 h at rt, then concentrated in vacuo. The crude product was used directly in the next step without further purification, (M+H) 144.1
Workup
- concentrationconcentrated in vacuo
- customThe crude product was used directly in the next step without further purification, (M+H) 144.1
Sources & evidence
- ORD record
- ord-d94c48da737f4d6c857d7cb73586e1c1
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09126927B2
Reaction notes
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