1,4-Dioxane hydrochloride → HCID 66642971, compound
Reaction equation
[CH2:1]([C:3]1([OH:17])[CH2:8][CH2:7][CH:6]([NH:9]C(=O)OC(C)(C)C)[CH2:5][CH2:4]1)[CH3:2].[ClH:18].O1CCOCC1>O1CCOCC1>[ClH:18].[NH2:9][CH:6]1[CH2:7][CH2:8][C:3]([CH2:1][CH3:2])([OH:17])[CH2:4][CH2:5]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a mixture of tert-butyl (4-ethyl-4-hydroxycyclohexyl)carbamate (Preparation Example 246) (0.202 g) and dioxane (2 mL), 26% hydrogen chloride-dioxane (1.1 mL) was added under ice cooling and stirred at room temperature for 12 hours. The solvent was distilled off to give 4-amino-1-ethylcyclohexanol hydrochloride (0.140 g) as a white viscous solid.
Workup
- additionwas added under ice cooling
- distillationThe solvent was distilled off
Sources & evidence
- ORD record
- ord-f871a6a79315464dbef728efa2472c10
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08969336B2
Reaction notes
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