Hydrochloric Acid → 1956306-41-4
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1([N:14]=C(C2C=CC=CC=2)C2C=CC=CC=2)[CH2:12][CH:11]2[O:13][CH:8]([CH2:9][CH2:10]2)[CH2:7]1)=[O:5])[CH3:2].[ClH:28]>C(OCC)C>[ClH:28].[CH2:1]([O:3][C:4]([C:6]1([NH2:14])[CH2:12][CH:11]2[O:13][CH:8]([CH2:9][CH2:10]2)[CH2:7]1)=[O:5])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A two-phase mixture of 3-(benzhydrylideneamino)-8-oxabicyclo[3.2.1]octane-3-carboxylic acid ethyl ester (1.4 grams, 3.9 mmol) in aqueous 1N hydrochloric acid solution (100 mL) and diethyl ether (100 mL) was stirred at room temperature overnight. The aqueous layer was concentrated to provide the title compound (0.70 grams, 78%, a 3:1 mixture of exo/endo diastereomers) as a pale yellow solid.
Workup
- concentrationThe aqueous layer was concentrated
Sources & evidence
- ORD record
- ord-4dcbce3c48f84e418a673cee0f8625ed
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06110964
Reaction notes
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