Hydrochloric Acid → 2-Cyclopentene-1-methanol, 4-amino-, hydrochloride (1:1), (1S,4R)-
Reaction equation
C([C@@:8]1([NH2:15])[CH2:12][C@H:11]([CH2:13][OH:14])[CH:10]=[CH:9]1)(OC(C)(C)C)=O.[ClH:16]>CO>[ClH:16].[NH2:15][C@@H:8]1[CH2:12][C@H:11]([CH2:13][OH:14])[CH:10]=[CH:9]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
87.8 g of (1R,4S)-1-BOC-amino-4-hydroxymethyl-2-cyclopentene were dissolved in 270 ml of 2N HCl and 1340 ml of methanol. The mixture was boiled under reflux for 4.5 h. After distillation of the methanol, the residue was dissolved in 800 ml of water. The aqueous solution was extracted twice with 340 ml of ethyl acetate. The aqueous phase was completely evaporated (50° C./60 mbar). The solid was dried at 50° C. in vacuo, suspended in 150 ml of diethyl ether, filtered off and washed twice with 50 ml of diethyl ether. Drying resulted in the title compound in a yield of 95% (58.4 g).
Workup
- temperatureunder reflux for 4.5 h
- distillationAfter distillation of the methanol
- dissolutionthe residue was dissolved in 800 ml of water
- extractionThe aqueous solution was extracted twice with 340 ml of ethyl acetate
- customThe aqueous phase was completely evaporated (50° C./60 mbar)
- customThe solid was dried at 50° C. in vacuo
- filtrationfiltered off
- washwashed twice with 50 ml of diethyl ether
- customDrying
Sources & evidence
- ORD record
- ord-2abe6052db8d4bdeaf6d5706d640c957
- Source dataset
- uspto-grants-2000_10
- Patent number
- US06137007
Reaction notes
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