1,4-Dioxane hydrochloride → 15833-88-2
Reaction equation
C(OC(=O)[NH:7][CH:8]1[C:12]([CH3:14])([CH3:13])[CH2:11][O:10][CH2:9]1)(C)(C)C.[ClH:16].O1CCOCC1>>[ClH:16].[CH3:13][C:12]1([CH3:14])[CH2:11][O:10][CH2:9][CH:8]1[NH2:7]Participants
3
Procedure
(4,4-Dimethyl-tetrahydro-furan-3-yl)-carbamic acid tert-butyl ester (70 mg, 0.32 mmol) was dissolved in 3 mL of cold 4M HCl/dioxane and gradually warmed to room temperature with stirring. After the starting material was judged to be consumed by thin layer chromatography, the reaction mixture was concentrated to afford 4,4-dimethyl-tetrahydro-furan-3-ylamine hydrochloride which was used with further purification.
Workup
- customto be consumed by thin layer chromatography
- concentrationthe reaction mixture was concentrated
Sources & evidence
- ORD record
- ord-c0edaea5c42d4b278c85eb25a68a2bca
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08329699B2
Reaction notes
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