Hydrochloric Acid → 2-(2-Aminoethyl)-1H-isoindole-1,3(2H)-dione--hydrogen chloride (1/1)
Reaction equation
C(OC([NH:8][CH2:9][CH2:10][N:11]1[C:15](=[O:16])[C:14]2=[CH:17][CH:18]=[CH:19][CH:20]=[C:13]2[C:12]1=[O:21])=O)(C)(C)C.[ClH:22]>C(OCC)(=O)C>[ClH:22].[NH2:8][CH2:9][CH2:10][N:11]1[C:15](=[O:16])[C:14]2=[CH:17][CH:18]=[CH:19][CH:20]=[C:13]2[C:12]1=[O:21]Participants
4
Procedure
A mixture of N-(2-tert-butoxycarbonylaminoethyl)phthalimide (2.5 g) and 4N solution of hydrogen chloride in ethyl acetate (25 ml) was stirred for 1 hour at ambient temperature. The resulting precipitates were collected by filtration and washed with ethyl acetate to give N-(2-aminoethyl)phthalimide hydrochloride (1.89 g) as colorless crystals.
Workup
- customThe resulting precipitates
- filtrationwere collected by filtration
- washwashed with ethyl acetate
Sources & evidence
- ORD record
- ord-088d5612d5cc4277bcff6be687a19dbe
- Source dataset
- uspto-grants-1999_12
- Patent number
- US06008229
Reaction notes
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