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(S)-2-tert-Butoxycarbonylamino-5-oxo-hexanoic acid ethyl ester → (S)-ethyl 5-methyl-3,4-dihydro-2H-pyrrole-2-carboxylate

HRID 1431831
Notes
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Reaction equation

HRID 1431831 reaction equation
C(OC([NH:8][C@@H:9]([CH2:15][CH2:16][C:17](=O)[CH3:18])[C:10]([O:12][CH2:13][CH3:14])=[O:11])=O)(C)(C)C>FC(F)(F)C(O)=O.ClCCl>[CH3:18][C:17]1[CH2:16][CH2:15][C@@H:9]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[N:8]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 58544329(S)-2-tert-Butoxycarbonylamino-5-oxo-hexanoic acid ethyl ester

Product 1

HCID 67682752(S)-ethyl 5-methyl-3,4-dihydro-2H-pyrrole-2-carboxylate

Reagents, catalysts & solvents 1

HCID 21863450Trifluoroacetic acid methylene chlorideSolvent

Procedure

(S)-ethyl 2-(tert-butoxycarbonylamino)-5-oxohexanoate in a 1 L flask was treated with a trifluoro acetic acid/dichloromethane solution (1:1 mixture, 100 mL). Effervescence was observed and the mixture was allowed to stir for 4 hours at room temperature. After which time the volatiles were removed in vacuo to yield (S)-ethyl 5-methyl-3,4-dihydro-2H-pyrrole-2-carboxylate as an oil, and used directly in the following step.

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  • customAfter which time the volatiles were removed in vacuo
  • Sources & evidence

    ORD record
    ord-4608b21e670747e4b9a6759905ff0fcd
    Source dataset
    uspto-grants-2015_01
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08940718B2

    Reaction notes

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