Hydrochloric Acid → HCID 15916372, compound
Reaction equation
[ClH:1].[F:2][CH2:3][CH:4]([NH:18]C(OC(C)(C)C)=O)[CH2:5][CH2:6][CH:7]([NH:10]C(OC(C)(C)C)=O)[C:8]#[CH:9]>CCOCC>[ClH:1].[ClH:1].[F:2][CH2:3][CH:4]([NH2:18])[CH2:5][CH2:6][CH:7]([NH2:10])[C:8]#[CH:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A saturated solution of dry hydrogen chloride in dry ether (10 ml) is added to 1-fluoro-2,5-di-(N-tert.butoxycarbonylamino)-6-heptyne obtained as in Step D above (1 mmole) and left overnight at room temperature. The dichlorohydride which forms as crystals is filtered, washed with ether, and dried to give the title compound (0.21 g).
Workup
- customobtained as in Step D above (1 mmole)
- filtrationis filtered
- washwashed with ether
- customdried
Sources & evidence
- ORD record
- ord-b6a2dcc9d4754c83ad3eaf65f83216d3
- Source dataset
- uspto-grants-1983_12
- Patent number
- US04421768
Reaction notes
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