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1,2-Bis(diphenylphosphino)ethane → Ethyl cis-1-benzyl-4-(1-tert-butoxycarbonylaminocyclopropyl)pyrrolidine-3-carboxylate

HRID 635099
Notes
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Reaction equation

HRID 635099 reaction equation
C1(P(C2C=CC=CC=2)CCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH2:29]([N:36]1[CH2:40][C:39]([C:41]2([NH:44][C:45]([O:47][C:48]([CH3:51])([CH3:50])[CH3:49])=[O:46])[CH2:43][CH2:42]2)=[C:38]([C:52]([O:54][CH2:55][CH3:56])=[O:53])[CH2:37]1)[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1>CO>[CH2:29]([N:36]1[CH2:40][C@H:39]([C:41]2([NH:44][C:45]([O:47][C:48]([CH3:50])([CH3:51])[CH3:49])=[O:46])[CH2:42][CH2:43]2)[C@H:38]([C:52]([O:54][CH2:55][CH3:56])=[O:53])[CH2:37]1)[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 742671,2-Bis(diphenylphosphino)ethaneHCID 21261012Ethyl 1-benzyl-4-(1-tert-butoxycarbonylaminocyclopropyl)-3-pyrroline-3-carboxylate

Product 1

HCID 69563544Ethyl cis-1-benzyl-4-(1-tert-butoxycarbonylaminocyclopropyl)pyrrolidine-3-carboxylateYield 97.8%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Under a nitrogen gas stream, bis(bicyclo[2.2.1]hepta-2,5-diene)rhodium (I) perchlorate (54.5 mg, 0.14 mmol) and 1,2-bis(diphenylphosphino)ethane (67.4 mg, 0.17 mmol) were dissolved in degassed methanol (25 ml) and stirred at room temperature for 10 minutes. To this catalyst solution was added a solution of ethyl 1-benzyl-4-(1-tert-butoxycarbonylaminocyclopropyl)-3-pyrroline-3-carboxylate (1.090 g, 2.820 mmol) in dry and degassed methanol (15 ml). The thus obtained liquid reaction mixture was then stirred under a hydrogen atmosphere (1 kg/cm2) at room temperature for 2.5 hours. After adding active carbon (1 g), the liquid reaction mixture was allowed to stand at room temperature for 30 minutes and then filtered.through celite (washed with methanol). The filtrate was concentrated under reduced pressure and the residue was subjected to flash silica gel column chromatography (eluent: n-hexane:ethyl acetate=5:1) to obtain 1.071 g (97.8%) of the title compound as colorless crystals.

Workup

  1. customin dry
  2. customdegassed methanol (15 ml)
  3. customThe thus obtained liquid reaction mixture
  4. stirringwas then stirred under a hydrogen atmosphere (1 kg/cm2) at room temperature for 2.5 hours
  5. additionAfter adding active carbon (1 g)
  6. customthe liquid reaction mixture
  7. waitto stand at room temperature for 30 minutes
  8. washfiltered.through celite (washed with methanol)
  9. concentrationThe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-39bb49e4d11844b58d8a96d76323aad8
Source dataset
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06184388B2

Reaction notes

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