Hydrochloric Acid → HCID 131713236, compound
Reaction equation
[F:1][CH2:2][CH:3]([NH:18]C(OC(C)(C)C)=O)[CH:4]([F:17])[CH2:5][N:6]1C(=O)C2=CC=CC=C2C1=O.[ClH:26]>>[ClH:26].[ClH:26].[F:1][CH2:2][CH:3]([NH2:18])[CH:4]([F:17])[CH2:5][NH2:6]Participants
3
Procedure
A mixture of 1,3-difluoro-2-tert.butoxycarbonylamino-4-phthalimidobutane (0.1 g, 0.27 mmol) obtained as in Step C above and concentrated hydrochloric acid is heated at 100° C. for 48 hours. The solvent is evaporated in vacuo and the residue is taken up in water. Insoluble phthalic acid is filtered off and the filtrate concentrated to yield 1,3-difluoro-2,4-diaminobutane, dihydrochloride (0.03 g).
Workup
- customobtained as in Step C above
- customThe solvent is evaporated in vacuo
- filtrationInsoluble phthalic acid is filtered off
- concentrationthe filtrate concentrated
Sources & evidence
- ORD record
- ord-7070f52082f044e1ab277f2e174f2d7e
- Source dataset
- uspto-grants-1983_11
- Patent number
- US04418077
Reaction notes
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