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Hydrochloric Acid → 1-(Prop-2-en-1-yl)piperazin-2-one

HRID 1162808
Notes
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Reaction equation

HRID 1162808 reaction equation
[CH2:1]([N:4]1[CH2:9][CH2:8][N:7](C(OC(C)(C)C)=O)[CH2:6][C:5]1=[O:17])[CH:2]=[CH2:3].Cl>CCOC(C)=O>[CH2:1]([N:4]1[CH2:9][CH2:8][NH:7][CH2:6][C:5]1=[O:17])[CH:2]=[CH2:3]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 544523841-(2-Propenyl)-4-tert-butyloxycarbonyl-2-piperazinone

Product 1

HCID 200992691-(Prop-2-en-1-yl)piperazin-2-one

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Conditions

Temperature
0 °C

Procedure

Into a stirred solution of 1-(2-propenyl)-4-tert-butyloxycarbonyl-2-piperazinone (11 g, 46 mmol) in EtOAc (100 mL) at 0° C. was bubbled HCl gas for 10 min. The mixture was stirred at 0° C. for 30 min and then at ambient temperature for 1 h. The solvent was removed in vacuo to yield the hydrochloride salt of the title compound as a white solid. ES MS (M+H)=141.

Workup

  1. waitat ambient temperature for 1 h
  2. customThe solvent was removed in vacuo

Sources & evidence

ORD record
ord-9300c0339c024c21ab4b2edce0e23cd6
Source dataset
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07820680B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes